[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"cardiac-catheterization\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:cardiac-catheterization":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,9,0,[8,49,77,100,123,149,174,200,228],{"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":4,"maxAge":17,"enrollmentInfo":57,"targetDuration":4,"studyType":59,"phases":4,"briefSummary":60,"conditions":61,"keywords":63,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":71,"completionDateStruct":73,"leadSponsor":75,"locationsCount":48},"100636349","efficacy-and-safety-of-a-combined-dexmedetomidine-ketamine-sedation-regimen-for-pediatric-cardiac-catheterization-100636349","NCT07564531","Efficacy and Safety of a Combined Dexmedetomidine-Ketamine Sedation Regimen for Pediatric Cardiac Catheterization","Evaluation of the Efficacy and Safety of a Combined Dexmedetomidine-Ketamine Sedation Regimen for Pediatric Cardiac Catheterization at Vietnam National Children's Hospital","KETADEX","Inclusion Criteria:\n\n* Patients under 18 years of age.\n* Patients indicated for diagnostic or interventional cardiac catheterization.\n\nExclusion Criteria:\n\n* Patients with acute respiratory infections, chromosomal abnormalities, metabolic disorders, or other co-existing medical conditions.\n* Arrhythmias, second- or third-degree atrioventricular (AV) block; patients on mechanical ventilation or requiring vasopressors prior to the procedure.\n* Known history of allergy or hypersensitivity to dexmedetomidine, ketamine, propofol, midazolam, or sevoflurane.",{"count":58,"type":20},150,"OBSERVATIONAL","The goal of this observational study is to learn if the spontaneous sedation regimen of dexmedetomidine-ketamine (KETADEX) has the comparable efficacy and safety in pediatric cardiac catheterization versus the traditional regimen. The main question it aims to answer is:\n\nIs the combined Dexmedetomidine-Ketamine spontaneous sedation regimen (KETADEX) non-inferior to the traditional general anesthesia regimen in terms of efficacy and safety?\n\nParticipants would received either KETADEX regimen or general anesthesia regimen. Research members then observe the catheterization procedure and answer the questionnaire about their efficacy and safety.",[28,62],"Pediatric",[64,65,66,67,68],"dexmedetomidine","ketamine","spontaneous sedation","general anesthesia","cardiac catheterization","2026-04-29",{"date":37,"type":40},{"date":72,"type":40},"2026-02-04",{"date":74,"type":20},"2026-12-30",{"name":76,"class":47},"National Children's Hospital, Vietnam",{"id":78,"slug":79,"hasResults":11,"nctId":80,"briefTitle":81,"officialTitle":82,"acronym":4,"eligibilityCriteria":83,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":84,"targetDuration":4,"studyType":59,"phases":4,"briefSummary":86,"conditions":87,"keywords":4,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":90,"lastUpdatePostDateStruct":91,"startDateStruct":93,"completionDateStruct":95,"leadSponsor":97,"locationsCount":48},"100570105","gsi-cardiac-on-revolution-apex---us-100570105","NCT06702917","GSI Cardiac on Revolution Apex - US","Wide Coverage GSI Cardiac Data Collection","Inclusion Criteria:\n\nSubjects may be included in this study if they meet the following criteria:\n\n1. Who are ≥18 years of age;\n2. Able to sign and date the informed consent form; AND,\n3. Cohort A: Undergoing a scheduled clinically indicated CCTA; OR,\n4. Cohort B: Known history of myocardial infarction or undergoing a clinically indicated cardiac catheterization due to known pathology.\n\nExclusion Criteria:\n\nSubjects may be excluded from participating in study if they meet any of the following criteria:\n\n1. Who are pregnant or lactating;\n2. Who were previously enrolled in this study;\n3. Anyone with known or suspected allergy to iodinated contrast agents;\n4. Anyone with known or suspected renal insufficiency as determined by site medical personnel;\n5. Who are in need of urgent or emergent care;\n6. Who have any conditions that, in the opinion of the PI or designee, would interfere with the evaluation of the results or constitute a health hazard for the subject;\n7. Who are unwilling to have GEHC personnel present for the CT exam; AND,\n8. Cohort A: Undergoing a scheduled clinically indicated CCTA for anatomy assessment (aberrant origin, etc.)",{"count":85,"type":20},50,"The goal of this clinical data collection study is to collect raw CT scan data using a new GSI Cardiac mode on GE HealthCare's Revolution Apex CT system.\n\nTwo groups of participants will be enrolled:\n\nA) Participants scheduled to undergo a Coronary CT Angiography (CCTA) as part of their standard of care\n\nB) Participants scheduled to undergo a cardiac catheterization or have a history of heart attack\n\nParticipants in Group A will:\n\n-Have a standard of care CCTA immediately followed by a research GSI Cardiac scan\n\nParticipants in Group B will:\n\n-Have a research CCTA immediately followed by a research GSI Cardiac scan\n\nBoth groups will be in the study for approximately 1 day. There are no follow-up visits after the day of scan.",[88,89,28],"Coronary Computed Tomographic Angiography","Myocardial Infarction (MI)","2026-04-24",{"date":92,"type":40},"2026-04-27",{"date":94,"type":40},"2025-09-10",{"date":96,"type":20},"2026-06",{"name":98,"class":99},"GE Healthcare","INDUSTRY",{"id":101,"slug":102,"hasResults":11,"nctId":103,"briefTitle":104,"officialTitle":105,"acronym":4,"eligibilityCriteria":106,"healthyVolunteers":11,"sex":16,"minAge":4,"maxAge":17,"enrollmentInfo":107,"targetDuration":4,"studyType":59,"phases":4,"briefSummary":109,"conditions":110,"keywords":4,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":114,"lastUpdatePostDateStruct":115,"startDateStruct":117,"completionDateStruct":119,"leadSponsor":121,"locationsCount":48},"100621821","a-multimodal-ai-prediction-model-for-complications-after-transcatheter-closure-of-perimembranous-vsd-in-children-100621821","NCT07375602","A Multimodal AI Prediction Model for Complications After Transcatheter Closure of Perimembranous VSD in Children","Multimodal Clinical Data Integration and Artificial Intelligence Modeling for Predicting Complications Following Pediatric Transcatheter Closure of Perimembranous Ventricular Septal Defect","Inclusion Criteria:\n\n* Age ≤ 18 years at the time of transcatheter procedure.\n* Diagnosis of perimembranous ventricular septal defect confirmed by echocardiography, and underwent transcatheter device closure at the study center.\n* Medical records sufficient to ascertain the primary outcome within the pre-specified follow-up window, and availability of minimum baseline clinical information required for model development\u002Fvalidation.\n\nExclusion Criteria:\n\n* Ventricular septal defects not classified as perimembranous on echocardiography, including muscular, outlet, or inlet VSDs, as well as multiple or complex VSDs involving more than one septal region.\n* Presence of complex congenital heart disease or associated structural abnormalities requiring concomitant surgical repair (e.g., tetralogy of Fallot).\n* Prior surgical VSD repair or prior transcatheter VSD closure.",{"count":108,"type":20},5249,"The goal of this observational study is to develop and validate a multimodal artificial intelligence prediction model for treatment-related complications in children with perimembranous ventricular septal defect (pmVSD) undergoing transcatheter device closure. The main question it aims to answer is: Can an AI model that integrates demographics, laboratory results, electronic health record text, echocardiography reports, chest radiographs, and electrocardiogram accurately predict the risk of complications at the individual patient level? Data will be retrospectively collected from routine clinical care records of pediatric patients who underwent transcatheter closure for pmVSD. Deep learning methods will be used to extract features from text and images to train and validate the prediction model.",[111,112,28,113],"Congenital Heart Disease (CHD)","Ventricular Septal Defects (VSD)","Postoperative Complications","2026-04-03",{"date":116,"type":40},"2026-04-09",{"date":118,"type":40},"2026-02-01",{"date":120,"type":20},"2026-06-15",{"name":122,"class":47},"Xinhua Hospital, Shanghai Jiao Tong University School of Medicine",{"id":124,"slug":125,"hasResults":11,"nctId":126,"briefTitle":127,"officialTitle":127,"acronym":4,"eligibilityCriteria":128,"healthyVolunteers":11,"sex":16,"minAge":129,"maxAge":130,"enrollmentInfo":131,"targetDuration":4,"studyType":21,"phases":133,"briefSummary":134,"conditions":135,"keywords":137,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":140,"lastUpdatePostDateStruct":141,"startDateStruct":143,"completionDateStruct":145,"leadSponsor":147,"locationsCount":48},"100511559","ultrasound-detectable-endotracheal-tube-a-feasibility-study-100511559","NCT05941013","Ultrasound-detectable Endotracheal Tube: a Feasibility Study","Inclusion Criteria:\n\n* Patient is undergoing scheduled or planned diagnostic or interventional cardiac catheterization with planned general anesthesia requiring endotracheal intubation.\n\nExclusion Criteria:\n\n* Patient has a known airway abnormality, including tracheal stenosis, previous tracheal stenosis, or tracheobronchomalacia.\n* Patient has a tracheostomy.\n* Patient is ventilator-dependent.\n* Patient has an anticipated difficult intubation based upon airway exam and\u002For history of difficult intubation.\n* Patient is unlikely (in opinion of anesthesia team) or is unable to be intubated with 3.5 mm, 4.0 mm, or 4.5 mm Inner Diameter USD-ETT due to the size of the patient or their airway.\n* Patient is already intubated prior to the scheduled procedure.\n* It is anticipated that the patient will not be extubated after the catheterization procedure.\n* Concurrent enrollment in another clinical trial with an intervention during the cardiac catheterization procedure or 30 days afterwards.\n* Allergy to plastic\u002Fmaterials in USD-ETT","6 Months","42 Months",{"count":132,"type":20},20,[23],"The researchers are studying whether special features make it easier to see if the breathing tube is in the correct place. It is hoped that the investigational device will enable more accurate placement (depth and trachea vs. esophagus).",[28,136],"Endotracheal Tube",[138,139],"Ultrasound","Intubation","2026-02-03",{"date":142,"type":40},"2026-02-05",{"date":144,"type":40},"2023-11-15",{"date":146,"type":20},"2027-04",{"name":148,"class":47},"John R. Charpie",{"id":150,"slug":151,"hasResults":11,"nctId":152,"briefTitle":153,"officialTitle":154,"acronym":4,"eligibilityCriteria":155,"healthyVolunteers":11,"sex":16,"minAge":156,"maxAge":4,"enrollmentInfo":157,"targetDuration":4,"studyType":21,"phases":159,"briefSummary":160,"conditions":161,"keywords":4,"overallStatus":164,"whyStopped":4,"lastUpdateSubmitDate":165,"lastUpdatePostDateStruct":166,"startDateStruct":168,"completionDateStruct":170,"leadSponsor":172,"locationsCount":4},"100617563","virtual-reality-for-patient-preparation-before-cardiac-catheterization-in-oman-100617563","NCT07320248","Virtual Reality for Patient Preparation Before Cardiac Catheterization in Oman","Evaluating the Efficacy of Virtual Reality in Patient Preparation for Cardiac Catheterization Procedures in Oman: A Randomized Controlled Trial","Inclusion Criteria:\n\n* • Adult patients (aged 18 years and above)\n\n  * Scheduled for first-time elective cardiac catheterization\n  * Able to understand Arabic or English\n  * Capable of providing informed consent\n\nExclusion Criteria:\n\n* • Individuals with cognitive impairment or psychiatric conditions that may interfere with their ability to engage in the VR intervention\n\n  * Patients requiring emergency or urgent catheterization","19 Years",{"count":158,"type":20},120,[23],"Background: Cardiovascular disease is considered one of the most prevalent diseases in recent times, and cardiac catheterization is widely used to diagnose and treat cardiovascular disease. However, patients often experience significant anxiety before the procedure due to fear of the unknown, potential complications, and concern about discomfort.Aim: To evaluate the efficacy of virtual reality technology to reduce anxiety and improve patient satisfaction, attitude, and usefulness in individuals undergoing first-time cardiac catheterization procedures in Oman.Method: A mixed-method randomized control trial will be used with approximately 120 patients from different tertiary hospitals in Oman. The experimental group will experience a virtual reality simulation of the catheterization process before providing informed consent, while the control group will receive the standard pre-procedure education. The Arabic version of the DASS-21 scale will be used to assess anxiety level pre- and post-intervention, while patient satisfaction will be measured through qualitative interviews with a subset of 10 participants.Result: ANOVA will be conducted to examine differences in anxiety and satisfaction scores between groups, and Pearson's correlation (r) will assess relationships between anxiety levels and satisfaction scores, while paired t-tests will be applied to compare anxiety levels before and after the intervention within groups. Additionally, multiple regression analysis will be employed to identify predictors of patient satisfaction and anxiety reduction, with a significance level set at p ≤ 0.05 for all statistical tests.Conclusion: The expected outcome of this study is that virtual reality-based education will significantly reduce pre-procedure anxiety and enhance patient satisfaction compared to standard education. Findings from this research may contribute to improving patient-centered care and developing innovative strategies to optimize emotional preparedness before cardiac catheterization procedures.",[162,163,28],"Coronary Artery Disease","Ischaemic Heart Desease","NOT_YET_RECRUITING","2025-12-21",{"date":167,"type":40},"2026-01-06",{"date":169,"type":20},"2026-03-05",{"date":171,"type":20},"2027-06-30",{"name":173,"class":47},"Sultan Qaboos University",{"id":175,"slug":176,"hasResults":11,"nctId":177,"briefTitle":178,"officialTitle":179,"acronym":180,"eligibilityCriteria":181,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":182,"targetDuration":4,"studyType":21,"phases":184,"briefSummary":185,"conditions":186,"keywords":188,"overallStatus":164,"whyStopped":4,"lastUpdateSubmitDate":192,"lastUpdatePostDateStruct":193,"startDateStruct":195,"completionDateStruct":196,"leadSponsor":198,"locationsCount":4},"100604535","benefits-of-no-fasting-compared-to-fasting-prior-to-elective-cardiac-catheterization-a-single-center-randomized-controlled-trial-100604535","NCT07150780","Benefits of no Fasting Compared to Fasting Prior to Elective Cardiac Catheterization: A Single-center Randomized-controlled Trial","Benefits of no FASTing Prior to Elective Cardiac CATHeterization (FAST CATH): A Single-center Randomized-controlled Trial Comparing a Non-fasting Pre-procedure Approach to the Standard of Care in Adults Undergoing Elective Cardiac Catheterization With Moderate Sedation","FAST CATH","Inclusion Criteria:\n\n* Willing to comply with all study procedures and remain in contact with the study team to complete study assessments for the duration of the study\n* Scheduled for an elective (non-urgent) cardiac catheterization\n* Age of 18 or older at the time of consent\n\nExclusion Criteria:\n\n* Adults unable to consent\n* Pregnant women\n* Incarceration\n* Non-English-speaking patients\n* Inability to eat by mouth\n* Patients requiring general anesthesia for cardiac catheterization\n* Inability to fast for at least 6 hours\n* Personal history of pulmonary aspiration, or other known cardiopulmonary anesthetic complication(s)\n* Urgent cardiac catheterization\n* Inability or unwillingness to comply with all study procedures\n* Previously enrolled in this study (patients may not be enrolled more than once for subsequent procedures)",{"count":183,"type":20},2000,[23],"More than one million cardiac catheterizations (CCs) are performed annually in the United States and the majority are elective. Current guidelines recommend no fasting prior to elective CC, however recent studies suggest that eating and drinking as desired prior to elective CCs involving moderate sedation is safe.\n\nThis project will study the potential benefits of allowing patients to eat before elective CCs. Participants will be randomly divided into two groups. One group will receive pre-op instructions to fast, and the other group will be allowed to eat and drink as desired prior to their CC. Researchers will compare these groups with regards to patient satisfaction and respiratory complications.",[162,28,187],"Cardiac Diseases",[189,190,191],"Cardiac catheterization","Fasting","Patient Satisfaction","2025-08-25",{"date":194,"type":40},"2025-09-02",{"date":94,"type":20},{"date":197,"type":20},"2028-02-10",{"name":199,"class":47},"Munson Medical Center",{"id":201,"slug":202,"hasResults":11,"nctId":203,"briefTitle":204,"officialTitle":205,"acronym":4,"eligibilityCriteria":206,"healthyVolunteers":11,"sex":16,"minAge":207,"maxAge":208,"enrollmentInfo":209,"targetDuration":4,"studyType":21,"phases":211,"briefSummary":212,"conditions":213,"keywords":214,"overallStatus":164,"whyStopped":4,"lastUpdateSubmitDate":219,"lastUpdatePostDateStruct":220,"startDateStruct":222,"completionDateStruct":224,"leadSponsor":226,"locationsCount":4},"100571997","acupressures-impact-on-pain-and-physiological-parameters-in-infants-undergoing-cardiac-catheterization-100571997","NCT06727526","Acupressure's Impact on Pain and Physiological Parameters in Infants Undergoing Cardiac Catheterization","The Effect of Acupressure on Pain and Physiological Parameters in Infants Before and After Cardiac Catheterization: a Randomized Placebo Controlled Trial","Inclusion Criteria:\n\n* Infants between 1 month and 12 months\n* Infants with congenital heart disease\n* Infants undergoing cardiac catheterization for the first time\n* Infants undergoing planned cardiac catheterization\n* Infants without acupressure experience\n* Infants whose parents volunteered to participate in the study\n\nExclusion Criteria:\n\n* Infants with complications during catheterization\n* Infants followed up in the intensive care unit after catheterization\n* Infants with any deformity or lesion in the acupressure area\n* Infants who have not received analgesics after catheterization\n* Infants who were not given analgesics within six hours before catheterization\n* Infants with neurodevelopmental disorders\n* Infants whose parents did not volunteer to participate in the study","1 Month","12 Months",{"count":210,"type":20},35,[23],"Acupressure, one of the traditional Chinese medicine practices dating back approximately 5,000 years, is a mind-body technique that can be independently applied by nurses. This practice involves applying pressure to specific points on the body to reduce pain. The pressure stimulates the release of substances such as endorphins, acetylcholine, norepinephrine, and dopamine, resulting in muscle relaxation, regulated blood circulation, and blocked pain signals at nerve endings, effectively reducing the sensation of pain. The aim of acupressure is to alleviate patient discomfort and improve quality of life by reducing the need for analgesics. Acupressure, which falls under the category of therapeutic massage, can be applied using the fingers and palms. According to its core philosophy, illness arises when the balance of energy flowing through body channels, called \"meridians,\" is disrupted. Because acupressure does not involve needles, it is a safe, effective, and economical technique that is easy to learn and apply. The World Health Organization (WHO) classifies acupressure as a supportive treatment within its list of \"treatable conditions.\" The technique involves applying pressure to the same point for 2-5 minutes. Stimulating specific points promotes the release of cytokines, such as endorphins, which play a role in pain reduction by blocking certain receptors on sensory nerve endings and thus preventing pain perception. Additionally, stimulating acupoints helps establish sympathetic and parasympathetic balance, supporting healthy homeostasis. Studies in the literature have investigated acupressure's positive effects on children's preoperative anxiety, postoperative pain severity, chemotherapy side effects, fatigue, sleep quality, asthma symptoms, and physical stress. In a study examining the impact of acupressure on procedural pain in infants prior to parenteral vaccinations, infants who received acupressure experienced lower pain levels and shorter crying durations. Similarly, a study investigating the effect of acupressure on acute pain during venous catheter insertion in children found that pain severity was lower among children who received acupressure. A systematic review examining the effects of acupressure on child health determined that acupressure is effective in alleviating procedural pain in children. The review emphasized that nurses should incorporate acupressure, a non-pharmacological method, into care practices for effective pain management in children. Despite evidence in the literature supporting acupressure's positive effects on pediatric health, no study has specifically examined its impact on pain and physiological parameters in children undergoing cardiac catheterization. Therefore, this thesis aims to investigate the effects of acupressure, applied before and after cardiac catheterization, on pain levels and physiological parameters in infants.",[28],[68,215,216,217,218],"congenital heart disease","Acupressure","nursing care","pain","2024-12-13",{"date":221,"type":40},"2024-12-17",{"date":223,"type":20},"2024-12-30",{"date":225,"type":20},"2025-12-30",{"name":227,"class":47},"Baskent University",{"id":229,"slug":230,"hasResults":11,"nctId":231,"briefTitle":232,"officialTitle":233,"acronym":234,"eligibilityCriteria":235,"healthyVolunteers":11,"sex":16,"minAge":236,"maxAge":237,"enrollmentInfo":238,"targetDuration":4,"studyType":21,"phases":239,"briefSummary":240,"conditions":241,"keywords":242,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":246,"lastUpdatePostDateStruct":247,"startDateStruct":249,"completionDateStruct":251,"leadSponsor":253,"locationsCount":48},"100553207","effect-of-animated-education-on-anxiety-and-vascular-complications-100553207","NCT06483087","Effect of Animated Education on Anxiety and Vascular Complications","The Effect of Animated Education Program on Anxiety, Vascular Complications, And Flat Time Among Children Undergoing Cardiac Catheterization","VAEdA","Inclusion Criteria:\n\n* aged between 6-12 years\n* admitted for their first scheduled cardiac catheterization non-emergency CC procedure.\n\nExclusion Criteria:\n\n* children with developmental delay\n* emergency CC because\n* having major hearing or visual difficulties\n* children have deteriorated health conditions before CC and need to be admitted for intensive care before undergoing CC\n* children who have bleeding disorders","6 Years","12 Years",{"count":19,"type":20},[23],"An animated education program about cardiac catheterization will be presented 24 hours to children in the intervention group before undergoing cardiac catheterization. While children in the control group will receive routine care. Dependent variables are (Anxiety 2 hours before undergoing cardiac catheterization, hematoma and bleeding at the catheterization site 2 hours post sheath removal, flat time post cardiac catheterization).",[28],[189,243,244,245],"Anxiety","bleeding","flat time","2024-06-30",{"date":248,"type":40},"2024-07-01",{"date":250,"type":40},"2024-03-01",{"date":252,"type":20},"2025-04-01",{"name":254,"class":47},"University of Jordan"]