[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"chest-tube\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:chest-tube":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,48,80],{"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":29,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100628142","virtual-reality-forest-sounds-and-patient-outcomes-during-chest-tube-removal-100628142",false,"NCT07457788","Virtual Reality Forest Sounds and Patient Outcomes During Chest Tube Removal","The Effect of Nature Sounds in a Virtual Reality Forest During Chest Tube Removal on Pain, Vital Signs, Comfort, and Patient Satisfaction","Inclusion Criteria:\n\n* Able to speak and understand Turkish\n* Willing to participate in the study\n* Aged 18 years or older\n* No auditory or visual impairments\n\nExclusion Criteria:\n\n* Patients with impaired orientation to time and place\n* Patients with migraine, vertigo, or dizziness\n* Illiterate patients","ALL","18 Years",{"count":19,"type":20},60,"ESTIMATED","INTERVENTIONAL",[23],"NA","The aim of this study is to investigate the effects of listening to nature sounds in a virtual reality forest on pain, vital signs, comfort, and patient satisfaction during chest tube removal. This study aims to determine whether there are significant differences in pain, comfort, patient satisfaction, and vital signs between the experimental and control groups during chest tube removal. \"In this study, a VR video featuring a relaxing forest environment with nature sounds will be used with a virtual reality headset. Patients will be exposed to both auditory and visual stimuli. It is anticipated that the findings of this randomized controlled experimental study will make a significant contribution to the literature and clinical",[26,27,28],"Chest Tube","Virtual Reality","Chest Tube Removal",[30,31,32,33,34],"pain","chest tube","patient satisfaction","comfort","vital signs","RECRUITING","2026-03-03",{"date":38,"type":39},"2026-03-09","ACTUAL",{"date":41,"type":39},"2025-12-01",{"date":43,"type":20},"2026-06",{"name":45,"class":46},"Uskudar University","OTHER",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":4,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":55,"targetDuration":4,"studyType":21,"phases":57,"briefSummary":58,"conditions":59,"keywords":64,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":70,"lastUpdatePostDateStruct":71,"startDateStruct":73,"completionDateStruct":75,"leadSponsor":77,"locationsCount":47},"100617511","comparison-of-chest-tube-wound-closure-comparison-between-purse-string-method-and-plug-method-100617511","NCT07319572","Comparison of Chest Tube Wound Closure: Comparison Between Purse String Method and Plug Method.","Optimizing Chest Tube Removal: A Comparison of Purse-string Suture Closure and Plug Method.","Inclusion criteria :\n\n1. All patients \\>18 years of age\n2. Patients undergoing chest tube insertion for traumatic causes including Pneumothorax, hemothorax and hemopneumothorax.\n\nExclusion criteria:\n\n1. Previous ipsilateral thoracic surgery\n2. Patients with large wounds necessitating suture closure\n3. Patients with bleeding disorders",{"count":56,"type":20},246,[23],"This prospective, comparative clinical study evaluates two techniques of chest tube wound closure-purse-string suture and the simple suture\u002Fplug method-to determine differences in cosmetic outcomes, wound complications, and overall patient satisfaction following chest tube removal. The study aims to identify the closure technique that provides optimal wound healing with fewer postoperative complications.",[60,61,26,28,62,63],"Pneumothorax","Hemothorax","Purse String","Plug Method",[65,66,67,60,68],"Purse-string","Plug method","Chest tube","hemothorax","NOT_YET_RECRUITING","2025-12-19",{"date":72,"type":39},"2026-01-06",{"date":74,"type":20},"2026-01-01",{"date":76,"type":20},"2026-12-31",{"name":78,"class":79},"Pakistan Institute of Medical Sciences","OTHER_GOV",{"id":81,"slug":82,"hasResults":11,"nctId":83,"briefTitle":84,"officialTitle":85,"acronym":86,"eligibilityCriteria":87,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":88,"enrollmentInfo":89,"targetDuration":4,"studyType":21,"phases":91,"briefSummary":92,"conditions":93,"keywords":97,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":102,"lastUpdatePostDateStruct":103,"startDateStruct":105,"completionDateStruct":106,"leadSponsor":108,"locationsCount":110},"100552324","impact-of-ambulatory-management-for-primary-spontaneous-pneumothorax-in-the-emergency-department-on-quality-of-life-100552324","NCT06471608","Impact of Ambulatory Management for Primary Spontaneous Pneumothorax in the Emergency Department on Quality of Life","Impact of Ambulatory Management for Primary Spontaneous Pneumothorax in the Emergency Department on Quality of Life: a Randomized Clinical Trial","EFFI-PNO","Inclusion Criteria:\n\n* Patients aged 18 to 50 years presenting to the emergency department with a 1st episode of right or left primary spontaneous pneumothorax (PSP) of large abundance diagnosed by chest X-ray or CT scan defined according to British Thoracic Society (BTS) recommendations as a detachment greater than 2 cm over the entire height of the axillary line.\n* Patient living less than an hour from hospital and able to be accompanied for the first 48 hours\n* Patient able to understand the aims and risks of the research and to give informed, dated and signed consent\n* Patient with Internet access and able to complete online questionnaires\n* Patient affiliated to or benefiting from a social health insurance\n\nExclusion Criteria:\n\n* Small pneumothorax (≤ 2cm)\n* Suffocating pneumothorax defined by the presence of signs of respiratory distress or hemodynamic failure with indication for emergency exsufflation\n* Patient on emergency oxygen or long-term oxygen therapy\n* Traumatic pneumothorax\n* Secondary spontaneous pneumothorax\n* Bilateral pneumothorax\n* Associated fluid effusion\n* Risk-benefit balance unfavorable to outpatient treatment (comorbidities, isolated patient, difficulty understanding monitoring instructions)\n* Patient living more than one hour from hospital\n* Patients living alone or unable to be accompanied on discharge for the first 48 hours\n* Patients under legal protection\n* Pregnant or breast-feeding women\n* Patient participating in a therapeutic interventional clinical trial or in a period of exclusion linked to previous participation in a clinical trial","50 Years",{"count":90,"type":20},386,[23],"Outpatient treatment of Primary Spontaneous Pneumothorax (PSP) compared to usual inpatient management could improve quality of care and represent a more efficient, generalizable and sustainable strategy.\n\nThis multicenter, cluster-controlled, randomized interventional study with stepped wedge implementation will evaluate the impact on quality of life (between inclusion, after drain placement, and 6 months) of an ambulatory strategy for the management of large abundance primary spontaneous pneumothorax in the emergency department, compared with usual care.",[94,95,96,26],"Primary Spontaneous Pneumothorax","Quality of Life","Ambulatory Care",[98,99,100,101],"Chest tube drainage","Primary spontaneous pneumothorax","Ambulatory management","Quality of life","2025-11-20",{"date":104,"type":39},"2025-11-26",{"date":41,"type":20},{"date":107,"type":20},"2030-07",{"name":109,"class":46},"University Hospital, Strasbourg, France",7]