[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"satisfaction-patient\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:satisfaction-patient":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,10,0,[8,49,84,120,152,184,211,238,266,295],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":31,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":48},"100560360","ultrasound-guided-transversus-abdominis-plan-tap-block-in-endovascular-cardiac-interventions-100560360",false,"NCT06576128","Ultrasound-Guided Transversus Abdominis Plan (TAP) Block in Endovascular Cardiac Interventions","Analgesic Effect of Ultrasound-Guided Transversus Abdominis Plan (TAP) Block in Femoral Endovascular Cardiac Interventions: A Prospective-randomized Study","Inclusion Criteria:\n\n* The patient is over 18 years of age\n* Coronary angiography, cardiac catheterization and percutaneous coronary intervention will be applied to the patient,\n* The above-mentioned procedures will be taken under elective conditions,\n* Providing an optimal image when imaging the patient with ultrasound,\n* INR\\\u003C 1.5\n* If the patient gives consent, S\u002Fhe will be included in the study.\n\nExclusion Criteria:\n\n* Patients under 18 years of age,\n* Patients treated under emergency conditions,\n* morbid obesity (BMI\\>35 kg\u002Fm2),\n* pregnant women,\n* New York Heart Association (NYHA) stage 4 patients with advanced decompensated heart failure,\n* Patients with symptoms such as redness, temperature increase, infection, hematoma in the application area before the procedure,\n* Patients with a history of allergy to local anesthetics,\n* Patients who cannot be communicated,\n* Those with severe psychosis or progressive neurological deficits and muscle disease,\n* Patients who do not consent to the application will be excluded from the study.","ALL","18 Years",{"count":19,"type":20},100,"ESTIMATED","INTERVENTIONAL",[23],"NA","Sensory innervation of the femoral region which is the entry point for endovascular cardiac interventions such as coronary angiography,cardiac catheterization and percutaneous coronary intervention is complex.It is thought that the ilioinguinal and iliohypogastric nerves contribute mostly.With transversus abdominis plane block(TAPB),it is planned to provide analgesia by creating a block in these nerve branches that contribute to the sensory innervation of the intervention area.In addition;it was aimed to investigate patient's and physician's satisfaction during the procedure.",[26,27,28,29,30],"Anesthesiology","Percutaneous Coronary Intervention","Cardiac Catheterization","Analgesia","Satisfaction, Patient",[32,33,34,27,28,35],"ultrasonography","anesthesiology","transversus abdominis plane block","analgesia","RECRUITING","2026-05-04",{"date":39,"type":40},"2026-05-08","ACTUAL",{"date":42,"type":40},"2024-09-10",{"date":44,"type":20},"2026-12-15",{"name":46,"class":47},"Istanbul University - Cerrahpasa","OTHER",1,{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":55,"eligibilityCriteria":56,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":57,"targetDuration":4,"studyType":59,"phases":4,"briefSummary":60,"conditions":61,"keywords":70,"overallStatus":74,"whyStopped":4,"lastUpdateSubmitDate":75,"lastUpdatePostDateStruct":76,"startDateStruct":78,"completionDateStruct":80,"leadSponsor":82,"locationsCount":48},"100624164","duke-virtual-integrated-workflow-100624164","NCT07406074","Duke Virtual IntEgrated Workflow","DUH Innovation Units","Duke VIEW","Inclusion Criteria:\n\n* Admission to the hospital on one of six clinical units\n\nExclusion Criteria:\n\n* Less than 18 years old",{"count":58,"type":20},10000,"OBSERVATIONAL","This quality improvement initiative aims to evaluate the implementation, utilization, and impact of virtual care technologies and workflows being implemented at Duke University Health System (DUHS). This project is embedded within operational workflows and is designed to inform strategic decision-making and resource allocation. The evaluation will focus on key performance indicators (KPIs) relevant to hospital operations and patient outcomes, including but not limited to: Length of Stay, Readmission Rates, Patient Satisfaction Scores, and Other Quality and Safety Metrics. These KPIs will be evaluated across three clinical units at Duke University Hospital, in which virtual care technologies are being implemented. These will be compared to three control units of similar characteristics. Differences in KPIs will be examined across all units over 12 months.",[62,63,64,65,66,67,68,30,69],"Falls Injury","Readmission Rates","CLABSI - Central Line Associated Bloodstream Infection","Catheter Associated Urinary Tract Infection","Hospital Acquired Pressure Injury","Venous Thromboembolism (VTE)","Nurses","Length of Stay",[71,72,73],"Virtual Care","Nursing","Inpatient","NOT_YET_RECRUITING","2026-02-09",{"date":77,"type":40},"2026-02-12",{"date":79,"type":20},"2026-02-04",{"date":81,"type":20},"2027-02-03",{"name":83,"class":47},"Duke University",{"id":85,"slug":86,"hasResults":11,"nctId":87,"briefTitle":88,"officialTitle":89,"acronym":4,"eligibilityCriteria":90,"healthyVolunteers":11,"sex":91,"minAge":17,"maxAge":4,"enrollmentInfo":92,"targetDuration":4,"studyType":21,"phases":94,"briefSummary":95,"conditions":96,"keywords":108,"overallStatus":74,"whyStopped":4,"lastUpdateSubmitDate":111,"lastUpdatePostDateStruct":112,"startDateStruct":114,"completionDateStruct":116,"leadSponsor":118,"locationsCount":48},"100607351","incidence-of-pruritus-using-intrathecal-fentanyl-versus-epidural-fentanyl-to-initiate-labour-analgesia-100607351","NCT07187427","Incidence of Pruritus Using Intrathecal Fentanyl Versus Epidural Fentanyl to Initiate Labour Analgesia.","Randomized Trial Comparing the Injection of Intrathecal Fentanyl Versus Epidural Fentanyl for the Initiation of Labour Analgesia on the Incidence of Pruritis.","Inclusion Criteria:\n\n* Age ≥ 18 years\n* Vaginal delivery\n* Gestational age ≥ 37 weeks\n* Requesting neuraxial analgesia\n* French or English language\n\nExclusion Criteria:\n\n* ASA score \\> 3\n* Allergy or contraindication to receiving opioids\u002Flocal anesthesia (morphine or fentanyl)\n* BMI \\> 40 kg\u002Fm²\n* Hepatic or renal failure,\n* Severe preeclampsia and signs of severity according to the criteria of the American College of Obstetricians and Gynecologists\n* Maternal hemorrhage (placental abruption, hepatic subcapsular hematoma,...)\n* Severe scoliosis\n* Biliary cholestasis or polymorphic eruption of pregnancy\n* Inability to provide informed consent, either secondary to mental or physical disability or a significant language barrier (inability to understand English or French)\n* Prior administration of an opioid or opioid misuse","FEMALE",{"count":93,"type":20},80,[23],"The purpose of this study is to investigate the effect of neuraxial analgesia initiation on the incidence of pruritus in laboring women. Specifically, this study aim to compare intrathecal fentanyl with epidural fentanyl in order to determine whether the epidural route is associated with a lower occurrence and severity of pruritus. By clarifying these differences, the research seek to optimize analgesic strategies during labor while minimizing opioid-related side effects",[97,98,99,100,101,30,102,103,104,105,106,107],"Pruritis","Hypotension Drug-Induced","Urinary Retention","Fetal Bradycardia During Labor","Nausea and Vomitting","Labor Analgesia","Neuraxial Opioid","Opioid Analgesic Adverse Reaction","Term Labour","Fentanyl Analgesia","Fentanyl Adverse Reaction",[109,110],"neuraxial opioid induced pruritus during labor","Intrathecal fentanyl versus Epidural fentanyl","2025-11-20",{"date":113,"type":40},"2025-11-26",{"date":115,"type":20},"2026-01",{"date":117,"type":20},"2027-05",{"name":119,"class":47},"St. Justine's Hospital",{"id":121,"slug":122,"hasResults":11,"nctId":123,"briefTitle":124,"officialTitle":125,"acronym":4,"eligibilityCriteria":126,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":127,"targetDuration":4,"studyType":21,"phases":129,"briefSummary":131,"conditions":132,"keywords":137,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":143,"lastUpdatePostDateStruct":144,"startDateStruct":146,"completionDateStruct":148,"leadSponsor":150,"locationsCount":48},"100451331","phase-4-evaluating-a-dropless-postoperative-regimen-after-cataract-surgery-in-a-vulnerable-county-hospital-population-100451331","NCT05157113","Evaluating a Dropless Postoperative Regimen After Cataract Surgery in a Vulnerable, County-hospital Population","Evaluating the Efficacy, Compliance, and Patient Satisfaction of a New Dropless Postoperative Regimen After Cataract Surgery in a Vulnerable, County-hospital Population","Inclusion criteria:\n\n* ZSFG patient initially seen in the eye clinic, approved by attending ophthalmologist for cataract surgery in both eyes due to visually significant cataracts, and who elects to have cataract surgery in both eyes.\n* Patients 18 years of age or older\n\nExclusion criteria:\n\n* Patients requiring bilateral simultaneous (same-day bilateral) cataract surgery\n* Patients with prior history of: endophthalmitis, advanced glaucoma, known history of intraocular pressure elevation due to steroids, prior intraocular surgery, cystoid macular edema\u002Fdiabetic macular edema\u002Fretinal edema noted in the past 12 months prior to cataract surgery\n* Patients with documented penicillin or cephalosporin allergy or intolerance\n* Patients requiring combined same day cataract and ophthalmic subspecialty procedure (eg; combined cataract and glaucoma, retina, or cornea surgery).\n* Patients who are pregnant or breastfeeding",{"count":128,"type":20},70,[130],"PHASE4","The current postoperative cataract surgery eye drop regimen used at Zuckerberg San Francisco General Hospital (ZSFG) is a significant burden for its patient population, contributing to high rates of non-adherence and the development of postoperative complications. The investigators propose to replace this complex regimen with a single administration of intraocular antibiotic and subconjunctival steroid at the time of surgery. This pilot study will obtain the preliminary data required to eventually fully evaluate this innovation in postoperative care in a safety-net population with respect to postoperative outcomes, patient compliance, and patient and caregiver satisfaction.",[133,134,135,136,30],"Cataract","Surgery","Compliance, Patient","Compliance, Medication",[138,139,140,141,142],"cataract surgery","post-operative care","vulnerable populations","compliance","patient satisfaction","2025-07-18",{"date":145,"type":40},"2025-07-23",{"date":147,"type":40},"2022-05-31",{"date":149,"type":20},"2026-06-01",{"name":151,"class":47},"University of California, San Francisco",{"id":153,"slug":154,"hasResults":11,"nctId":155,"briefTitle":156,"officialTitle":157,"acronym":158,"eligibilityCriteria":159,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":160,"enrollmentInfo":161,"targetDuration":4,"studyType":21,"phases":163,"briefSummary":164,"conditions":165,"keywords":168,"overallStatus":74,"whyStopped":4,"lastUpdateSubmitDate":174,"lastUpdatePostDateStruct":175,"startDateStruct":177,"completionDateStruct":179,"leadSponsor":181,"locationsCount":183},"100580494","intercostal-nerve-block-for-pain-management-after-uniportal-video-assisted-thoracoscopic-surgeries-100580494","NCT06838026","Intercostal Nerve Block for Pain Management After Uniportal Video-assisted Thoracoscopic Surgeries","Internal, External Intercostal Nerve Block and Intercostal Catheter for Pain Management After Uniportal VATS: A Clinical Trial","VATS","Inclusion Criteria:\n\n* All participants between the ages of 18 and 80 year-old who have elective or urgent uniportal VATS will be included in the sample.\n\nExclusion Criteria:\n\n* Children - under the age of 18 or participants above the age of 80.\n* Participants with chest wall infections and those with decorticated lungs will be excluded from the study.\n* Participants with pre-existing chest pain or severe renal or hepatic dysfunction\n* Participants with a history of psychiatric disorder or inability to understand the consent form or how to use a Numerical Rating Scale (NRS) for pain measurement\n* Participants who have allergy to any of the given drugs, second thoracic surgery, participation in other clinical trials, obesity with body mass index\\>35 kg\u002Fm2, intake of antiplatelet or anticoagulant agents, spinal deformity and severe bradycardia will also be excluded.\n* Participants will be withdrawn from the study if the technical failure happened in the block or VATS procedure was converted to open procedure.","80 Years",{"count":162,"type":20},90,[23],"The goal of this clinical trial is to compare the safety and effectiveness of the three intercostal nerve blocks used in pain management in uniportal (one port) thoracoscopic surgeries: internal intercostal nerve blocks (ICNB), external ICNB, and Intercostal catheters.\n\nParticipants will be randomly assigned to three groups:\n\n* First group will undergo internal intercostal nerve block\n* Second group will be given external intercostal nerve block\n* Third group will have an intercostal catheter Researchers will compare the three groups to see their impact on post-operative pain management in uniportal VATS.",[166,167,29,30],"Thoracic","Pain, Postoperative",[169,170,171,172,173],"Intercostal nerve block","Intercostal Catheter","Video-Assisted Thoracoscopic Surgery","Post-operative Pain","Patients' Satisfaction","2025-03-26",{"date":176,"type":40},"2025-04-01",{"date":178,"type":20},"2025-05-05",{"date":180,"type":20},"2026-12-05",{"name":182,"class":47},"Al-Quds University",2,{"id":185,"slug":186,"hasResults":11,"nctId":187,"briefTitle":188,"officialTitle":189,"acronym":4,"eligibilityCriteria":190,"healthyVolunteers":11,"sex":91,"minAge":17,"maxAge":4,"enrollmentInfo":191,"targetDuration":4,"studyType":21,"phases":192,"briefSummary":193,"conditions":194,"keywords":199,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":202,"lastUpdatePostDateStruct":203,"startDateStruct":205,"completionDateStruct":207,"leadSponsor":209,"locationsCount":48},"100576803","impact-of-patient-selected-visual-art-in-the-hospital-room-during-antepartum-admission-on-hospital-satisfaction-scores-and-patient-experience-100576803","NCT06790043","Impact of Patient Selected Visual Art in the Hospital Room During Antepartum Admission on Hospital Satisfaction Scores and Patient Experience","Randomized Control Trial: Impact of Patient Selected Visual Art in the Hospital Room During Antepartum Admission on Hospital Satisfaction Scores and Patient Experience.","Inclusion Criteria:\n\n* patients who are greater than or equal to 18 years of age\n* patients admitted to the study hospital's antepartum unit for care\n* currently pregnant\n* willing and able to provide informed consent and complete the provided questionnaire\n\nExclusion Criteria:\n\n* patients less than 18 years of age\n* patients who are not pregnant\n* patients who are not admitted to study hospital's antepartum unit\n* patients who cannot provide informed consent in English\n* patients who have participated in this study during a previous admission",{"count":19,"type":20},[23],"The purpose of this study is to assess whether patient-selected visual art for patients admitted to the antepartum unit will increase hospital satisfaction compared to routine care.",[195,196,197,198,30],"Pregnancy","Pregnancy Complications","Hospital Environment","Hospitalization",[200,201],"Visual Art","Antepartum Hospitalization","2025-02-18",{"date":204,"type":40},"2025-02-19",{"date":206,"type":40},"2025-01-01",{"date":208,"type":20},"2026-12",{"name":210,"class":47},"Albany Medical College",{"id":212,"slug":213,"hasResults":11,"nctId":214,"briefTitle":215,"officialTitle":216,"acronym":4,"eligibilityCriteria":217,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":160,"enrollmentInfo":218,"targetDuration":4,"studyType":21,"phases":220,"briefSummary":221,"conditions":222,"keywords":4,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":229,"lastUpdatePostDateStruct":230,"startDateStruct":232,"completionDateStruct":234,"leadSponsor":236,"locationsCount":48},"100570242","postoperative-analgesia-between-paravertebral-block-and-epidural-block-in-esophageal-surgery-100570242","NCT06704698","Postoperative Analgesia Between Paravertebral Block and Epidural Block in Esophageal Surgery","Paravertebral Block With Liposomal Bupivacaine and Epidural Block With Plane Bupivacaine for Postoperative Analgesia in Esophageal Surgery: A Randomized, Non-inferiority Study","Inclusion Criteria:\n\n* American Society of Anesthesiologist physical status I-III;\n* Scheduled elective thoracoscopic esophagectomy(three-incision approach);\n* Approved participation before study.\n\nExclusion Criteria:\n\n* Patients with contraindications for local nerve block such as spinal anatomic structure abnormality or local infection of puncture area;\n* Anergic to medications used in this study;\n* Patient have chronic pain;\n* Patient receiving anticoagulants, opioids or have a history of narcotic abuse or alcohol abuse;\n* Inability to complete postoperative pain assessments or questionnaires due to communication barriers or mental disorders;",{"count":219,"type":20},132,[23],"Prevention of postoperative pain is essential for the recovery of esophageal surgery. Epidural analgesia is a traditional and standard perioperative pain management for these patients. Beneficials of epidural analgesia have been widely established. However, there are still several potential disadvantages such as perioperative hypotension, failure of administration, rare but serious neurological complications. Ultrasound-guided regional nerve block has become a widely used technique due to its low degree of trauma and precise target of action. In combined with liposome bupivacaine (LB), a new long-acting local anesthetic, was proven to have a maximum duration of 72 hours, thus improving postoperative analgesia, reducing opioid consumption, and enhancing patient satisfaction. The aim of this study was to evaluate the efficacy of TPVB liposomal bupivacaine (LB) or plane bupivacaine (SB) for Overall Benefit of Analgesic Score (OBAS) after esophageal surgery.",[223,224,225,226,227,228,30],"Pain Syndrome","Dizziness","Vomiting","Itching","Sweet Syndrome","Cold","2024-12-23",{"date":231,"type":40},"2024-12-30",{"date":233,"type":40},"2024-12-03",{"date":235,"type":20},"2025-12-30",{"name":237,"class":47},"Zhejiang Cancer Hospital",{"id":239,"slug":4,"hasResults":11,"nctId":240,"briefTitle":241,"officialTitle":242,"acronym":4,"eligibilityCriteria":243,"healthyVolunteers":244,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":245,"targetDuration":4,"studyType":21,"phases":247,"briefSummary":248,"conditions":249,"keywords":252,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":257,"lastUpdatePostDateStruct":258,"startDateStruct":260,"completionDateStruct":262,"leadSponsor":264,"locationsCount":183},"100564498","NCT06629961","Impact of Transepithelial Abutment Connection and Disconnection in Dental Implants","Impact of Connection and Disconnection of the Transepithelial Abutment in Dental Implants","Inclusion Criteria:\n\n* Healthy partially edentulous adult patients needing at least two implants for the placement of single or consecutive crowns in the posterior mandible or maxilla will be recruited.\n* These patients should exhibit a plaque index and gingival bleeding index of less than 25%, and have sufficient bone height and width for the placement of dental implants measuring 8 or 10 mm in length and 3.5 or 4 mm in diameter.\n* Additionally, they must have at least 2 mm of keratinized vestibular gingiva, stable occlusion, and a periodontium in good health\n\nExclusion Criteria:\n\n* Edentulous areas requiring bone grafts will be excluded.\n* Patients with medical conditions contraindicating implant surgery, such as severe bruxism or inadequate oral hygiene.\n* Pregnant or lactating women, patients undergoing bisphosphonate therapy, those receiving chemotherapy or radiotherapy in the head and neck area, non-compliant patients with incomplete data records, and those who do not attend regular follow-up appointments will also be excluded.",true,{"count":246,"type":20},32,[23],"Over the past decade, implant research has focused on maintaining the health and stability of peri-implant tissues. A key factor is platform switching at the bone level, where a narrower abutment than the implant is used. This technique increases the implant's horizontal surface area for biological width establishment and reduces stress on the crestal bone.\n\nStudies showed that repeated disconnection and reconnection of prosthetic components could compromise the mucosal barrier around implants, leading to an apical shift in the connective tissue junction and vertical tissue loss. This led to the \"one abutment, one time\" protocol, advocating the placement of the definitive abutment during initial implant surgery to avoid its removal during healing.\n\nA recent meta-analysis indicated bone loss at the marginal level due to abutment connection and disconnection, despite different treatment protocols. Thus, a standardized abutment between the fixed prosthesis and the implant has been recommended to preserve marginal bone levels. This approach moves the biological width apically, protecting the bone from irritation and improving marginal bone isolation.\n\nHowever, comparative evidence between direct implant-connected prostheses and trans-epithelial abutments is lacking. This study aims to evaluate the \"one abutment, one time\" protocol's effect on bone loss 12 months after prosthesis placement.\n\nSecondary objectives include assessing patient satisfaction using Patient-Reported Outcome Measures (PROM) during prosthesis fabrication and placement, and obtaining information on the diversity and function of microorganisms on the implant using metagenomic techniques 12 months post-prosthesis placement.\n\nThroughout the prosthesis fabrication and the first 12 months, various evaluations will be conducted in both abutment and Ti-base groups:\n\n* \\*\\*Bleeding:\\*\\* Recorded during various prosthetic stages.\n* \\*\\*Pain:\\*\\* Assessed using a visual analog scale after each stage.\n* \\*\\*Anesthesia:\\*\\* Recorded if used at each stage.\n* \\*\\*Radiographs:\\*\\* Number taken to check the fit.\n* \\*\\*Time:\\*\\* Measured for each prosthetic phase.\n* \\*\\*Repetitions:\\*\\* Number of repeated procedures quantified.\n* \\*\\*Metagenomic tests:\\*\\* Samples collected following the Human Microbiome Project protocol to analyze microbial diversity and function.",[250,251,30],"Bone Loss","Bacterium; Agent",[253,254,255,256],"bone loss","bacteria","dental implant","satisfaction","2024-10-10",{"date":259,"type":40},"2024-10-15",{"date":261,"type":20},"2024-11-01",{"date":263,"type":20},"2025-11-01",{"name":265,"class":47},"University of Valencia",{"id":267,"slug":268,"hasResults":11,"nctId":269,"briefTitle":270,"officialTitle":271,"acronym":4,"eligibilityCriteria":272,"healthyVolunteers":244,"sex":91,"minAge":17,"maxAge":4,"enrollmentInfo":273,"targetDuration":4,"studyType":21,"phases":275,"briefSummary":276,"conditions":277,"keywords":280,"overallStatus":74,"whyStopped":4,"lastUpdateSubmitDate":286,"lastUpdatePostDateStruct":287,"startDateStruct":289,"completionDateStruct":291,"leadSponsor":293,"locationsCount":4},"100557969","informative-video-to-alleviate-anxiety-and-improve-satisfaction-in-elective-caesarean-section-100557969","NCT06545019","Informative Video to Alleviate Anxiety and Improve Satisfaction in Elective Caesarean Section","Study of Informative Video On Alleviating Perioperative Anxiety And Improving Satisfaction Score In Obstetric Patient Undergoing Elective Lower Segment Caesarean Section Under Spinal Anaesthesia","Inclusion Criteria:\n\n* All obstetric patients American Society of Anaesthesiologists (ASA) II-III\n* First time undergo elective caesarean section\n* Under spinal anaesthesia.\n\nExclusion Criteria:\n\n* Less than 18 years old\n* ASA IV\n* known antenatal diagnosis of morbid foetal conditions\n* history of psychiatry illness",{"count":274,"type":20},75,[23],"Title:\n\n\"Study of Informative Video on Alleviating Perioperative Anxiety and Improving Satisfaction Score in Obstetric Patients Undergoing Elective Lower Segment Caesarean Section Under Spinal Anaesthesia\"\n\nObjective:\n\nThis study aims to evaluate the effectiveness of an informative video in reducing perioperative anxiety and enhancing satisfaction in obstetric patients undergoing elective Caesarean sections under spinal anaesthesia. The hypothesis is that patients who view the video will experience lower anxiety and higher satisfaction compared to those who receive standard pre-anaesthetic counselling alone.\n\nBackground:\n\nSpinal anaesthesia, commonly used for Caesarean sections, offers rapid, predictable pain relief but can cause discomfort due to factors such as visceral pain and fundal pressure, leading to perioperative anxiety. Anxiety can negatively impact maternal satisfaction and increase the risk of postpartum complications. Previous studies have shown mixed results regarding the efficacy of educational videos in alleviating this anxiety.\n\nMethods:\n\nThe study is a prospective, randomized controlled trial conducted at Universiti Malaya Medical Centre. Eligible participants are obstetric patients (ASA II-III) undergoing elective Caesarean sections. Participants are randomly assigned to either an intervention group, which receives a supplemental informative video, or a control group receiving standard care. Anxiety and satisfaction levels are assessed using validated questionnaires pre- and post-surgery.\n\nAnticipated Outcomes:\n\nThe study hypothesizes that the informative video will significantly reduce perioperative anxiety and improve maternal satisfaction, thereby demonstrating the superiority of this intervention over standard pre-anaesthetic counselling.",[278,279,30],"Pre-operative Anxiety","Spinal Anesthesia",[281,282,283,284,285,279],"Informative Video","Perioperative Alleviation of Anxiety","Maternal Satisfaction","Preoperative Education","Elective Cesarean Section","2024-08-20",{"date":288,"type":40},"2024-08-23",{"date":290,"type":20},"2024-08-15",{"date":292,"type":20},"2025-06-15",{"name":294,"class":47},"University of Malaya",{"id":296,"slug":297,"hasResults":11,"nctId":298,"briefTitle":299,"officialTitle":300,"acronym":301,"eligibilityCriteria":302,"healthyVolunteers":244,"sex":16,"minAge":17,"maxAge":303,"enrollmentInfo":304,"targetDuration":306,"studyType":59,"phases":4,"briefSummary":307,"conditions":308,"keywords":4,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":324,"lastUpdatePostDateStruct":325,"startDateStruct":327,"completionDateStruct":329,"leadSponsor":331,"locationsCount":48},"100498046","safe-brain-initiative-operationalizing-precision-anaesthesia-100498046","NCT05765162","Safe Brain Initiative, Operationalizing Precision Anaesthesia","Safe Brain Initiative - Dedicated to Advancing Anaesthesia and Perioperative Personalised Care Towards Precision Anaesthesia Care. A Continuous Quality Improvement Initiative.","SBI","Inclusion Criteria:\n\n• All patients from age ≥18\n\nExclusion Criteria:\n\n• All patients from age \\\u003C18","100 Years",{"count":305,"type":20},15000,"5 Years","Perioperatively, patients experience an unnecessarily high level of side effects associated with their treatment. These side effects include nausea, severe pain, anxiety, and stress. Moreover, many patients develop postoperative delirium (POD) and neurocognitive dysfunctions, often resulting in long-term cognitive impairment, decreased quality of life, and increased mortality. However, physicians, nurses and their institutions do not receive structured feedback regarding these aspects of each patient's well-being. They may therefore be unable to engage in the essential cause-and-effect learning necessary to evaluate and consecutively reduce such side effects.\n\nEffective guidelines conform prevention is the proven key to shielding our patients from adverse Outcomes. The Safe Brain Initiative's high-quality routine data-for-action is a sword and accelerator for moving towards patient-centred, precision care. Thus, establishing a foundation for value-based and patient-centred healthcare development.\n\nHowever, a turnkey real-world solution is challenging to develop and implement and requires substantial resources. As a result, such solutions are usually beyond the scope of a single institution. The SBI platform provides high-quality, real-world data to bridge this gap. It allows monitoring and in-depth analysis of cause and effect in the day-to-day routine of individuals, departments, and institutions.\n\nThe SBI's approach is continuously improved and updated. An organization called the SBI Global Society oversees the quality and precision of science through experts in the field. At SBI Hospitals and Flagship centres, Masterclasses are conducted and can be attended alongside clinical immersions.\n\nSBI Solutions manages, develops, and provides technical and service support for the Safe Brain Initiative. Its service guarantees the professional and GDPR conform management of data handling and storage as well as the user-friendly functionality of the SBI-Dashboard solutions.",[309,310,311,312,225,313,314,315,316,317,318,319,30,320,321,322,323],"Neurocognitive Disorders","Post Operative Delirium","Pain","Nausea","Wellbeing","Shivering","Anxiety","Stress","Agitation,Psychomotor","Sedation Complication","Thirst","Temperature Change, Body","Fasting","Sore-throat","Hearing and Vision Loss","2024-06-05",{"date":326,"type":40},"2024-06-07",{"date":328,"type":40},"2021-12-01",{"date":330,"type":20},"2026-01-01",{"name":332,"class":47},"University of Southern Denmark"]