[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"vats\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:vats":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,10,0,[8,45,73,98,122,148,175,200,230,252],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100642769","acute-effects-of-visual-feedback-assisted-inspiratory-muscle-training-after-lobectomy-100642769",false,"NCT07646288","Acute Effects of Visual Feedback-Assisted Inspiratory Muscle Training After Lobectomy","Evaluation of the Acute Effects of Respiratory Muscle Strength Training With Visual Feedback in Lung Cancer Patients Undergoing Lobectomy","Inclusion Criteria:\n\n* Volunteering to participate in the study,\n* Being clinically stable,\n* Being a lung cancer patient scheduled for lobectomy,\n* Being between 18 and 75 years of age,\n* Being able to cooperate with the tests to be performed.\n\nExclusion Criteria:\n\n* Presence of any orthopedic or neurological problem that prevents walking,\n* History of any surgery involving the thoracic wall,\n* Having diseases that may affect respiratory parameters, such as severe heart failure or severe chronic obstructive pulmonary disease (COPD).","ALL","18 Years","75 Years",{"count":20,"type":21},40,"ESTIMATED","INTERVENTIONAL",[24],"NA","This study aims to evaluate the acute effects of inspiratory muscle training performed with and without a mobile application providing visual feedback on exercise motivation, patient adherence, dyspnea perception, usability, and patient satisfaction in lung cancer patients undergoing lobectomy via video-assisted thoracic surgery. Participants will perform conventional inspiratory muscle training without visual feedback in the morning on postoperative day 1 after transfer to the ward. After at least two hours of rest, the same exercise protocol will be repeated with a smart adaptor connected to a mobile application to provide visual feedback. Inspiratory muscle training will be performed using a threshold-loading device at 40% of maximal inspiratory pressure, with three sets of ten breaths. Outcomes will be assessed before and\u002For after each session as appropriate.",[27,28,29,30,31],"VATS","Respiratory Muscles","Exercise Training","Lung Cancer (NSCLC)","Lobectomy","RECRUITING","2026-06-11",{"date":35,"type":36},"2026-06-15","ACTUAL",{"date":38,"type":36},"2025-12-01",{"date":40,"type":21},"2027-03-01",{"name":42,"class":43},"Hacettepe University","OTHER",1,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":4,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":52,"enrollmentInfo":53,"targetDuration":4,"studyType":55,"phases":4,"briefSummary":56,"conditions":57,"keywords":61,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":64,"lastUpdatePostDateStruct":65,"startDateStruct":67,"completionDateStruct":68,"leadSponsor":70,"locationsCount":44},"100637381","analgesic-efficiency-of-sipspb-vs-icnb-in-vats-surgery-100637381","NCT07577908","Analgesic Efficiency of SIPSPB vs ICNB in VATS Surgery","Comparison Of The Analgesic Effectiveness Of Ultrasonography-Guided Serratus Posterıor Superior Intercostal Plane (SPSIP) Block And Intercostal Nerve (ICN) Block In Video-Assisted Thoracoscopic Surgery Patients","Inclusion Criteria:\n\n* Aged 18-80 years,\n* American Society of Anesthesiologists (ASA) physical status I-III\n* Patients who have provided informed consent to participate in the study\n\nExclusion Criteria:\n\n* Patients who refuse to participate in the study by not signing the informed consent\n* Patients classified as ASA \\> 3, according to the system established by the American Society of Anesthesiologists\n* Patients unable to understand the use of the NPR Scale or the PCA device that will be used for postoperative analgesia\n* Coagulation disorders or anticoagulant therapy contraindicating regional anesthesia\n* Patients with allergies to analgesic and\u002For anesthetic drugs\n* Infection at the block injection site\n* Patients whose surgical procedure is intraoperatively converted to an open pulmonary resection","80 Years",{"count":54,"type":21},80,"OBSERVATIONAL","This study aims to evaluate the effectiveness of Serratus Posterior Superior Intercostal Plane (SPSIP) block compared to Intercostal Nerve (ICN) block in terms of postoperative pain control, reduction of opioid analgesic consumption, minimization of postoperative respiratory complications, and increase patient satisfaction (using a 5-point Likert scale) in patients undergoing video-assisted thoracoscopic surgery (VATS).",[58,59,60,27],"Intercostal Nerve Block","Serratus Posterior Superior Intercostal Plane Block","Post-operative Pain Management",[62,63,27],"Serratus posterior superior intercostal plane block","intercostal nerve block","2026-05-18",{"date":66,"type":36},"2026-05-20",{"date":64,"type":36},{"date":69,"type":21},"2026-08-01",{"name":71,"class":72},"Kocaeli City Hospital","OTHER_GOV",{"id":74,"slug":75,"hasResults":11,"nctId":76,"briefTitle":77,"officialTitle":78,"acronym":4,"eligibilityCriteria":79,"healthyVolunteers":11,"sex":16,"minAge":80,"maxAge":81,"enrollmentInfo":82,"targetDuration":4,"studyType":22,"phases":83,"briefSummary":84,"conditions":85,"keywords":4,"overallStatus":88,"whyStopped":4,"lastUpdateSubmitDate":89,"lastUpdatePostDateStruct":90,"startDateStruct":92,"completionDateStruct":94,"leadSponsor":96,"locationsCount":4},"100608295","subxiphoid-vats-for-giant-mediastinal-teratoma-100608295","NCT07199699","Subxiphoid VATS for Giant Mediastinal Teratoma","The Safety and Efficacy of Subxiphoid Minimally Invasive Resection of Giant Mediastinal Teratoma Assisted by Double Sternal Elevation","Inclusion Criteria:\n\n* Age: 10 - 70 years old, gender unrestricted; Preoperative enhanced CT or MRI confirms anterior mediastinal mass with the maximum diameter ≥ 7 cm; Intraoperative frozen section pathology confirms teratoma (mature or immature type); American Society of Anesthesiologists (ASA) classification grade I - III, with acceptable cardiopulmonary function for single-lung ventilation; No severe thoracic deformity or severe adhesion in the posterior mediastinum (assessed by preoperative imaging); Patients voluntarily sign the informed consent form, understanding the purpose and potential risks of the study.\n\nExclusion Criteria:\n\n* Tumors invading major blood vessels (such as the innominate vein, superior vena cava, or aorta) or the pericardium require combined vascular\u002Fpericardial resection and reconstruction; Tumors crossing the midline and encasing the trachea or esophagus require multidisciplinary joint surgery; Previous mediastinal surgery or radiotherapy history, leading to local anatomical structure disorder; Coagulation dysfunction (INR \\> 1.5 or platelet count \\\u003C 50×10⁹\u002FL); Severe immune deficiency (such as HIV infection, long-term glucocorticoid treatment); Pregnant or lactating women; Concurrent other malignant tumors (metastatic lesions need to be excluded); Severe cardiopulmonary diseases (such as COPD GOLD Ⅲ-Ⅳ grade, NYHA cardiac function Ⅲ-Ⅳ grade); Mental illness or cognitive impairment that cannot cooperate with postoperative follow-up; Participated in other clinical trials that may interfere with the results of this study.","10 Years","70 Years",{"count":20,"type":21},[24],"For giant mediastinal teratomas, the only treatment option available is usually open-chest surgery, which causes significant trauma, leads to obvious postoperative pain and may result in long-term complications such as chest wall deformity. Currently, we have developed a new treatment method. We use a double retractor system to pull the upper and lower ends of the sternum, lifting it to obtain sufficient surgical space behind the sternum. This enables us to perform minimally invasive tumor resection through the subxiphoid approach with thoracoscopy. The advantages of this method include reduced surgical trauma and postoperative pain, shortened hospital stay, and improved cosmetic effect",[86,87,27],"Teratomas","Mediastinal ( Chest) Masses","NOT_YET_RECRUITING","2025-09-26",{"date":91,"type":36},"2025-09-30",{"date":93,"type":21},"2025-11-01",{"date":95,"type":21},"2027-06-30",{"name":97,"class":43},"Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine",{"id":99,"slug":100,"hasResults":11,"nctId":101,"briefTitle":102,"officialTitle":102,"acronym":4,"eligibilityCriteria":103,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":81,"enrollmentInfo":104,"targetDuration":4,"studyType":22,"phases":106,"briefSummary":107,"conditions":108,"keywords":110,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":113,"lastUpdatePostDateStruct":114,"startDateStruct":116,"completionDateStruct":118,"leadSponsor":120,"locationsCount":44},"100580495","assessing-the-impact-of-additional-serratus-anterior-block-within-24-hour-on-postoperative-pain-after-rhomboid-intercostal-block-in-vats-patients-100580495","NCT06838039","Assessing the Impact of Additional Serratus Anterior Block Within 24-Hour on Postoperative Pain After Rhomboid Intercostal Block in VATS Patients","Inclusion Criteria:\n\n1. Adults aged 18-70 years.\n2. Patients undergoing Video-Assisted Thoracoscopic Surgery (VATS).\n3. Classified as ASA physical status I-III (low to moderate surgical risk).\n4. Ability to provide informed consent and follow study protocols.\n\nExclusion Criteria:\n\n1. Known allergy or hypersensitivity to local anesthetics.\n2. Presence of bleeding disorders or anticoagulant use.\n3. History of chronic opioid use or opioid dependence.\n4. Anatomical abnormalities or conditions preventing the application of regional anesthesia (e.g., chest wall deformities).\n5. Presence of neurological disorders affecting pain perception.\n6. Cognitive impairments, language barriers, or inability to communicate effectively.\n7. Pregnancy or breastfeeding.\n8. Refusal or inability to provide informed consent.",{"count":105,"type":21},50,[24],"Title: Assessing the Impact of Additional Serratus Anterior Block on Postoperative Pain After Rhomboid Intercostal Block in VATS Patients\n\nPurpose: This randomized controlled trial aims to evaluate whether the addition of a Serratus Anterior Plane Block (SAPB) to the standard Rhomboid Intercostal Block (RIB) improves postoperative pain management in patients undergoing Video-Assisted Thoracoscopic Surgery (VATS).\n\nStudy Design:\n\n* Type: Randomized Controlled Trial (RCT)\n* Participants: 50 patients aged 18 -70 requiring VATS, randomized into two groups: one receiving RIB alone, and the other receiving RIB + SAPB.\n* Duration: Pain and opioid consumption will be measured within 48 hours post-surgery.\n* Outcome Measures: Pain levels using the Visual Analog Scale (VAS), opioid usage, and patient satisfaction.\n\nSignificance:\n\nThe study addresses the gap in research regarding the combined use of SAPB and RIB in pain control for VATS. It hypothesizes that the combination will lead to better pain relief and reduced opioid dependence compared to RIB alone.",[109,27],"Post Operative Pain",[111,112],"Postoperative Pain Management","Video-Assisted Thoracoscopic Surgery","2025-08-22",{"date":115,"type":36},"2025-08-28",{"date":117,"type":36},"2025-04-01",{"date":119,"type":21},"2026-12-01",{"name":121,"class":43},"Al-Quds University",{"id":123,"slug":124,"hasResults":11,"nctId":125,"briefTitle":126,"officialTitle":127,"acronym":128,"eligibilityCriteria":129,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":52,"enrollmentInfo":130,"targetDuration":4,"studyType":22,"phases":132,"briefSummary":133,"conditions":134,"keywords":138,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":139,"lastUpdatePostDateStruct":140,"startDateStruct":142,"completionDateStruct":144,"leadSponsor":146,"locationsCount":44},"100597985","tubeless-vats-for-mediastinal-neoplasm-100597985","NCT07065604","Tubeless VATS for Mediastinal Neoplasm","A Randomized Controlled Trial of Non-intubated Versus Intubated VATS for Mediastinal Neoplasm","NOVA-02","Inclusion Criteria:\n\n1. Mediastinal neoplasm was diagnosed by chest enhanced CT\n2. The patients with age ≥ 18 and ≤ 80 years old\n3. The patients whose tumor diameter was \\\u003C6 cm\n4. ASA grade: I-III\n5. The patients should understand the research and sign the informed consent\n\nExclusion Criteria:\n\n1. Imaging examinations revealed that the tumor had invaded adjacent organs, with evidence of pleural or pericardial dissemination, as well as lymphatic and\u002For hematogenous metastases\n2. Patients with a confirmed history of congestive heart failure, poorly controlled angina despite medical therapy, electrocardiogram-confirmed myocardial infarction with transmural involvement, uncontrolled hypertension, clinically significant valvular heart disease, or high-risk arrhythmias not adequately managed\n3. Patients with concurrent active malignancies",{"count":131,"type":21},132,[24],"In recent year, non-intubated anesthesia had emerged as an available and promising alternative for thoracic procedure. However, its safety and feasibility in video-assisted thoracoscopic surgery (VATS) for mediastinal neoplasm remain controversial. This randomized controlled trial is designed to evaluate the impact of the non-intubated approach on surgical and perioperative outcomes in patients undergoing mediastinal neoplasm resection.",[135,27,136,137],"Mediastinal Neoplasm","Tubeless","Non-intubated Anesthesia",[137,136,135,27],"2025-07-04",{"date":141,"type":36},"2025-07-15",{"date":143,"type":36},"2025-03-26",{"date":145,"type":21},"2028-08-31",{"name":147,"class":43},"Shuben Li",{"id":149,"slug":150,"hasResults":11,"nctId":151,"briefTitle":152,"officialTitle":153,"acronym":4,"eligibilityCriteria":154,"healthyVolunteers":11,"sex":16,"minAge":155,"maxAge":4,"enrollmentInfo":156,"targetDuration":4,"studyType":22,"phases":158,"briefSummary":159,"conditions":160,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":166,"lastUpdatePostDateStruct":167,"startDateStruct":169,"completionDateStruct":171,"leadSponsor":173,"locationsCount":44},"100520200","optimal-postoperative-chest-tube-and-pain-management-in-patients-surgically-treated-for-primary-spontaneous-pneumothorax-pneumotrial-100520200","NCT06053476","Optimal Postoperative Chest Tube and Pain Management in Patients Surgically Treated for Primary Spontaneous Pneumothorax (Pneumotrial)","Optimal Postoperative Chest Tube and Pain Management in Patients Surgically Treated for Primary Spontaneous Pneumothorax (Pneumotrial); a Randomized Controlled Trial","Inclusion Criteria:\n\n* All patients operated for PSP\n* Age ≥ 16 years\n* Able to read and understand the Dutch language\n* Mentally able to provide informed consent\n* Patients should have a preoperative chest CT scan in order to exclude evident secondary pneumothorax. Previously made CT scans, within a time range of maximum 5 years, are accepted. The identification of blebs or bullae on CT scan is not defined as secondary pneumothorax.\n\nExclusion Criteria:\n\n* Previous ipsilateral thoracic surgery (except diagnostic thoracoscopy only) or ipsilateral thoracic radiotherapy\n* Underlying lung disease that provoked the pneumothorax (secondary pneumothorax): genetically proven Birt-Hogg-Dubé syndrome, periodic pneumothorax in female patients in reproductive age with known endometriosis (or known catamenial pneumothorax), pulmonary cystic fibrosis, active pneumonia, lung fibrosis, chronic obstructive pulmonary disease (COPD), pulmonary ipsilateral malignancy\n* Contra-indications for TEA (infection at skin site, increased intracranial pressure, non-correctable coagulopathy, sepsis and mechanical spine obstruction)\n* Patients chronically (\\>3 months) using opioids will be excluded since postoperative baseline opioid requirement will be higher and TEA remains the preferred technique for these patients\n* Allergic reactions to analgesics used in the study","16 Years",{"count":157,"type":21},366,[24],"Guidelines lack high quality evidence on optimal postoperative chest tube and pain management after surgery for primary spontaneous pneumothorax (PSP). This results in great variability in postoperative care and length of hospital stay (LOS). Chest tube and pain management are prominent factors regarding enhanced recovery after thoracic surgery, and in standardised care they are crucial to improve quality of recovery and decrease LOS.\n\nHistorically, postoperative chest tubes are left in place for at least a fixed number of 3-5 days, irrespective of absence of air leakage. This period was deemed necessary for adequate pleurodesis and prevention of recurrence. However, it is suggested that removal on the same day of surgery is safe and associated with a reduced LOS.\n\nRegarding postoperative pain management, thoracic epidural analgesia (TEA) is the gold standard for postoperative pain management following video-assisted thoracic surgery (VATS). Although the analgesic effect of TEA is clear, it is associated with hypotension and urinary retention. Therefore, unilateral regional techniques, such as paravertebral blockade (PVB), are developed.\n\nThe investigators hypothesize that early chest tube removal accompanied by a single-shot paravertebral blockade (PVB) for analgesia is safe regarding pneumothorax recurrence and non-inferior regarding pain, but superior regarding LOS when compared to standard conservative treatment.",[161,27,162,163,164,165],"Pneumothorax, Primary Spontaneous","Pain, Postoperative","Locoregional Anaesthesia","Thoracic Epidural","Chest Tube Drainage","2025-05-06",{"date":168,"type":36},"2025-05-09",{"date":170,"type":36},"2023-11-08",{"date":172,"type":21},"2028-11-01",{"name":174,"class":43},"Maxima Medical Center",{"id":176,"slug":177,"hasResults":11,"nctId":178,"briefTitle":179,"officialTitle":180,"acronym":4,"eligibilityCriteria":181,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":182,"targetDuration":4,"studyType":22,"phases":184,"briefSummary":185,"conditions":186,"keywords":188,"overallStatus":88,"whyStopped":4,"lastUpdateSubmitDate":191,"lastUpdatePostDateStruct":192,"startDateStruct":194,"completionDateStruct":196,"leadSponsor":198,"locationsCount":44},"100586209","effect-of-transauricular-vagus-nerve-stimulation-on-postoperative-pain-management-in-video-assisted-thoracic-surgery-100586209","NCT06912399","Effect of Transauricular Vagus Nerve Stimulation on Postoperative Pain Management in Video Assisted Thoracic Surgery","Effect of Transauricular Vagus Nerve Stimulation on Postoperative Pain Management in Video Assisted Thoracic Surgery: a Randomized Controlled Clinical Trial","Inclusion Criteria:\n\n1. Age 18 years or older;\n2. ASA classification I-III;\n3. No prior taVNS treatment;\n4. Scheduled to undergo VATS (including segmentectomy and lobectomy);\n5. VAS ≥ 30 mm at any time on the day of surgery;\n6. Patients and their families can understand the study design and are willing to cooperate and participate in the study.\n\nExclusion Criteria:\n\n1. Psychiatric disorders or other conditions that prevent cooperation;\n2. Long-term use of steroids or opioids;\n3. Scheduled for bilateral VATS surgery;\n4. History of thoracic surgery;\n5. History of chronic pain, autoimmune diseases, or persistent infections.\n\nWithdrawl Criteria:\n\n1. Patient request;\n2. Surgery cancellation or change in surgical method resulting in failure to meet inclusion criteria;\n3. Severe perioperative complications and adverse events;\n4. Severe intervention-related adverse events.",{"count":183,"type":21},116,[24],"Transcutaneous auricular vagus nerve stimulation (taVNS) is a novel pain management technique that has gained popularity in recent years due to its non-invasive nature and ease of operation. Current literature has substantiated its efficacy in managing pain syndromes and chronic pain. However, there is a paucity of evidence regarding its effectiveness in treating acute postoperative pain. This project aims to explore the efficacy of taVNS in postoperative pain management, with a focus on video-assisted thoracic surgery(VATS). The investigators have designed a double-blind, single-center, randomized controlled clinical trial, planning to enroll 116 patients scheduled to undergo VATS(including segmentectomy or lobectomy) under general anesthesia at Peking Union Medical College Hospital. Participants will be divided into an intervention group (receiving taVNS) and a sham intervention group (receiving sham-taVNS), and will undergo a 2-hour intervention on the first postoperative day. The primary outcome is the pain relief rate, defined as a reduction of 15mm or 30% in the VAS (1-100mm) score immediately before and after the intervention on the first postoperative day. Secondary outcomes include: the proportion of patients with inadequate analgesia within three days after intervention; the difference in VAS scores immediately before and after the intervention on the first postoperative day; the incidence of opioid-related and taVNS-related side effects from the first to the third postoperative day after intervention; the number of effective and ineffective PCA presses (if used) from the first to the third postoperative day after intervention; the specifics and frequency of additional analgesic measures taken by patients from the first to the third postoperative day after intervention; the difference in RCSQ scores on the night of surgery and the night after intervention; and the probability of patients experiencing surgery-related pain three months after surgery. Follow-up period for this study will be three months after surgery.",[187,27],"Postoperative Pain, Acute",[189,190,27],"TaVNS","Postopearvie pain","2025-03-30",{"date":193,"type":36},"2025-04-04",{"date":195,"type":21},"2025-03-25",{"date":197,"type":21},"2026-12-30",{"name":199,"class":43},"Peking Union Medical College Hospital",{"id":201,"slug":202,"hasResults":11,"nctId":203,"briefTitle":204,"officialTitle":205,"acronym":206,"eligibilityCriteria":207,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":208,"targetDuration":210,"studyType":55,"phases":4,"briefSummary":211,"conditions":212,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":220,"lastUpdatePostDateStruct":221,"startDateStruct":223,"completionDateStruct":225,"leadSponsor":227,"locationsCount":229},"100565166","prolonged-hospital-stay-after-thoracoscopic-anatomical-lung-resections-100565166","NCT06638645","Prolonged Hospital Stay After Thoracoscopic Anatomical Lung Resections","Reasons for Prolonged Hospital Stay After Thoracoscopic Anatomical Lung Resections","PROTRACT","Inclusion Criteria:\n\n* Patients referred for elective minimally invasive (uniportal or multiportal video- or robot-assisted) anatomical lung resection (lobectomy or segmentectomy)\n* Informed consent obtained pre-operatively\n* Age 18 years or older\n\nExclusion Criteria:\n\n* Patients younger than 18 years old\n* Traumatic event as indication for lung resection\n* Non-anatomical lung resections\n* Thoracotomy\n* Patients already hospitalized for other pathologies, pre-existent and not related to the lung surgery\n* Urgent\u002Femergency procedures",{"count":209,"type":21},140,"2 Months","In this study, the reasons for prolonged hospital stay after thoracoscopic (video- or robot-assisted) anatomical lung resections are investigated. Currently, whenever possible, these anatomical lung resections are performed thoracoscopically, as they offer significant improvements in terms of postoperative pain, number of postoperative complications, rehabilitation, tolerance for adjuvant chemotherapy, and length of hospital stay. The development of an 'Enhanced Recovery After Surgery' (ERAS) protocol for lung surgery has further reduced hospital stay and the need for opioids for analgesia. Despite the optimal implementation of the ERAS protocol, there are still patients who need to stay in the hospital longer than the median. The aim of this research is to investigate the reasons for this.",[213,27,214,215,216,217,218,219],"Minimally Invasive Surgical Procedures","RATS Surgery","Pulmonary Lobectomy","Pulmonary Segmentectomy","Air Leakage","Postoperative Complication","Pain Postoperative","2025-01-13",{"date":222,"type":36},"2025-01-15",{"date":224,"type":36},"2024-11-12",{"date":226,"type":21},"2025-12-31",{"name":228,"class":43},"University Hospital, Ghent",2,{"id":231,"slug":232,"hasResults":11,"nctId":233,"briefTitle":234,"officialTitle":234,"acronym":4,"eligibilityCriteria":235,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":236,"targetDuration":4,"studyType":22,"phases":238,"briefSummary":239,"conditions":240,"keywords":4,"overallStatus":88,"whyStopped":4,"lastUpdateSubmitDate":243,"lastUpdatePostDateStruct":244,"startDateStruct":246,"completionDateStruct":248,"leadSponsor":250,"locationsCount":44},"100575933","implementing-music-therapy-for-video-assisted-thoracoscopic-surgery-patients-a-quality-improvement-initiative-100575933","NCT06778720","Implementing Music Therapy for Video-Assisted Thoracoscopic Surgery Patients: A Quality Improvement Initiative","Inclusion Criteria:\n\n* Adults aged 18 years and older with lung mass diagnosis undergoing VATS\n\nExclusion Criteria:\n\n* Individuals with dementia, neurocognitive disorders, or chronic pain conditions.",{"count":237,"type":21},20,[24],"The purpose of this project is to introduce and implement music therapy as an evidence-based pain management protocol focused on reducing postoperative pain levels among Video-Assisted Thoracoscopic Surgery (VATS) patients in the Post-Anesthesia Care Unit (PACU) of the project site. The clinical question guiding this initiative is: In adult patients undergoing a VATS procedure, does the implementation of music therapy lead to lower postoperative pain scores in the PACU compared to no intervention within an 8-week timeframe? The investigator will ask eligible patients their immediate pain scores upon arrival into the PACU and then start music of patient's choice via over-the-ear headphones. Pain scores will be rechecked 30 minutes after implementation of music therapy. The standard of care pain medications and\u002For usual care will not be withheld or altered after surgery in lieu of music therapy.",[241,27,242],"Pain Assessment","Music Therapy","2025-01-12",{"date":245,"type":36},"2025-01-16",{"date":247,"type":21},"2025-01-14",{"date":249,"type":21},"2025-03-10",{"name":251,"class":43},"Cedars-Sinai Medical Center",{"id":253,"slug":254,"hasResults":11,"nctId":255,"briefTitle":256,"officialTitle":257,"acronym":4,"eligibilityCriteria":258,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":259,"targetDuration":4,"studyType":22,"phases":261,"briefSummary":263,"conditions":264,"keywords":272,"overallStatus":88,"whyStopped":4,"lastUpdateSubmitDate":292,"lastUpdatePostDateStruct":293,"startDateStruct":295,"completionDateStruct":297,"leadSponsor":299,"locationsCount":44},"100562399","phase-1-reinforced-and-non-reinforced-staple-lines-in-fissureless-lobectomy-100562399","NCT06602661","Reinforced and Non-Reinforced Staple Lines in Fissureless Lobectomy","A Prospective Randomized Study of Reinforced Vs Non-reinforced Staple Lines in Fissureless Lobectomy","Inclusion Criteria:\n\n* Patients aged 18 and over.\n* Patients undergoing fissureless lobectomy for lung carcinoma.\n\nExclusion Criteria:\n\n* Patients suitable for sub lobar resections.\n* Patients undergoing lobectomy for indications other than lung cancer.\n* Patients with a history of pleural adhesions.\n* Patients with previous lung resection on the same side.",{"count":260,"type":21},65,[262],"PHASE1","Prolonged Air Leak (PAL) is a common and serious problem after lung surgery. It can lead to worse patient outcomes, longer hospital stays, and higher costs. Reinforced staplers are designed to make the staple line stronger and reduce the risk of PAL. However, investigators don't know if they are better than standard staplers, especially in a specific type of lung surgery called fissureless lobectomy for lung cancer. This study aims to find out if reinforced staplers are more effective at reducing PAL and its complications compared to non-reinforced staplers.\n\nReinforced staplers have been used in lung surgeries and have shown to reduce PAL. For example, staplers with special materials like polyglycolic acid (PGA) sheets have shown lower air leakage and fewer days with chest tubes. Other materials like expanded polytetrafluoroethylene (ePTFE) sleeves have also been used to manage air leaks in different types of lung surgeries. However, their effectiveness in fissureless lobectomy has not been studied yet.",[265,266,267,268,269,31,270,271,27],"Lung","Lung Adenocarcinoma","Lung Adenosquamous Carcinoma","Lung Cancer, Non-Small Cell","Lung Carcinoma","Lobectomy Patient","Lobectomy by Video-thoracoscopies",[273,274,275,276,277,269,278,279,280,281,282,283,284,285,286,287,288,289,290,291],"Prospective Randomized Study","Fissureless Lobectomy","Prolonged Air Leak (PAL)","Pulmonary Resections","Hospital Length of Stay (LOS)","Echelon 3000 stapler","Endopath Stapler Line Reinforcement","Video-Assisted Thoracoscopic Surgery (VATS)","Postoperative Outcomes","Intraoperative Characteristics","Randomized Control Trial (RCT)","Surrey Memorial Hospital (SMH)","Surrey Thoracic Surgery Group (STSG)","Digital Drainage System (Thopaz)","Chest Tube Duration","Hospital Readmission","Patient Outcomes","Bioabsorbable Buttress Material","Polyglactin and Polydioxanone","2024-09-17",{"date":294,"type":36},"2024-09-19",{"date":296,"type":21},"2025-01-01",{"date":298,"type":21},"2028-01",{"name":300,"class":43},"Surrey Thoracic Surgery Group"]