[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"thoracic-surgical-procedures\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:thoracic-surgical-procedures":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,47,75,103],{"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":29,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100649395","transcutaneous-electrical-nerve-stimulation-for-acute-postoperative-pain-after-video-assisted-thoracoscopic-surgery-100649395",false,"NCT07732764","Transcutaneous Electrical Nerve Stimulation for Acute Postoperative Pain After Video-Assisted Thoracoscopic Surgery","Effects of Transcutaneous Electrical Nerve Stimulation on Acute Postoperative Pain, Sleep Quality, and Quality of Life in Patients Undergoing Video-Assisted Thoracoscopic Surgery: A Randomized, Double-Blind, Sham-Controlled Study","Inclusion Criteria\n\n* Aged 15 to 85 years.\n* Participants younger than 18 years of age must have written informed consent provided by a parent or legal guardian.\n* Able to communicate and read\u002Fwrite in Chinese.\n* Scheduled to undergo video-assisted thoracoscopic surgery (VATS) as determined by the treating physician.\n* Have stable vital signs.\n* Willing to participate in the study and able to complete all study procedures.\n\nExclusion Criteria\n\n* History of a bleeding disorder.\n* Patients undergoing emergency surgery.\n* Patients undergoing bilateral video-assisted thoracoscopic surgery (VATS).\n* History of cardiac disease, including cardiac arrhythmia or implantation of a cardiac pacemaker.\n* Known allergy or hypersensitivity to TENS electrodes or adhesive pads.\n* Cognitive impairment or inability to comply with the study procedures","ALL","15 Years","85 Years",{"count":20,"type":21},90,"ESTIMATED","INTERVENTIONAL",[24],"NA","This randomized, double-blind, sham-controlled study aims to evaluate the effects of transcutaneous electrical nerve stimulation (TENS) on acute postoperative pain, sleep quality, and quality of life in patients undergoing video-assisted thoracoscopic surgery (VATS). Participants will be randomly assigned to either an active TENS group or a sham TENS group. TENS treatment will be administered twice daily for 30 minutes over three consecutive days beginning 24 hours after surgery. Pain intensity, sleep quality, and quality of life will be assessed at predefined time points to determine the effectiveness of TENS as an adjunctive postoperative pain management strategy.",[27,28],"Acute Postoperative Pain","Thoracic Surgical Procedures",[30,31,32,33,27],"Sleep Quality","Quality of Life","Video-Assisted Thoracoscopic Surgery (VATS)","Transcutaneous Electrical Nerve Stimulation (TENS)","RECRUITING","2026-07-26",{"date":37,"type":38},"2026-07-29","ACTUAL",{"date":40,"type":38},"2025-08-28",{"date":42,"type":21},"2026-10",{"name":44,"class":45},"Fooyin University","OTHER",1,{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":4,"eligibilityCriteria":53,"healthyVolunteers":11,"sex":16,"minAge":54,"maxAge":4,"enrollmentInfo":55,"targetDuration":4,"studyType":22,"phases":57,"briefSummary":58,"conditions":59,"keywords":64,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":46},"100643642","clinical-study-of-a-new-treatment-model-for-elderly-lung-cancer-patients-100643642","NCT07632664","Clinical Study of a New Treatment Model for Elderly Lung Cancer Patients","A Multicenter Clinical Study on a New Treatment Model Combining New Surgical Techniques, Perioperative Comprehensive Treatment, and Postoperative Rehabilitation for Elderly Patients With Lung Cancer","Inclusion Criteria:\n\n1. Aged ≥65 years old\n2. Pathologically confirmed non-small cell lung cancer with clinical stage eligible for curative surgical resection\n3. Complete preoperative geriatric comprehensive assessment data available\n4. Capable of finishing planned surgery and long-term follow-up\n5. Voluntarily sign informed consent form\n\nExclusion Criteria:\n\n1. History of other malignant tumors within recent 5 years\n2. Severe organic dysfunction of heart, liver, renal or respiratory system that cannot tolerate thoracic surgery\n3. Preoperative confirmed distant metastasis preventing radical resection\n4. Uncontrolled active severe infection or obvious coagulation disorders\n5. Severe psychiatric disorder or cognitive dysfunction failing to cooperate with treatment and follow-up\n6. Refuse random grouping and postoperative regular monitoring","65 Years",{"count":56,"type":21},1000,[24],"This multicenter prospective clinical study focuses on elderly patients with lung cancer. The investigators will build a standardized clinical registry database, develop perioperative risk stratification and surgical early-warning models, optimize individualized surgical regimens, construct multidisciplinary perioperative comprehensive therapy, integrated Chinese-Western medicine full-cycle management and personalized postoperative rehabilitation systems, so as to form a whole-process optimized treatment model for elderly lung cancer.",[60,28,61,62,63],"Lung Neoplasm","Perioperative Care","Postoperative Rehabilitation","Aged",[65],"Elderly lung cancer, Risk stratification, Multimodality therapy, Integrated Chinese and Western Medicine, Enhanced recovery after surgery","2026-07-14",{"date":68,"type":38},"2026-07-15",{"date":70,"type":38},"2024-08-01",{"date":72,"type":21},"2028-08-31",{"name":74,"class":45},"Peking University People's Hospital",{"id":76,"slug":77,"hasResults":11,"nctId":78,"briefTitle":79,"officialTitle":80,"acronym":81,"eligibilityCriteria":82,"healthyVolunteers":83,"sex":16,"minAge":84,"maxAge":4,"enrollmentInfo":85,"targetDuration":4,"studyType":87,"phases":4,"briefSummary":88,"conditions":89,"keywords":4,"overallStatus":93,"whyStopped":4,"lastUpdateSubmitDate":94,"lastUpdatePostDateStruct":95,"startDateStruct":97,"completionDateStruct":99,"leadSponsor":101,"locationsCount":4},"100646660","prevalence-and-risk-factors-for-chronic-post-surgical-pain-following-video-assisted-thoracic-surgery--the-evatho-prospective-bicentric-cohort-study-100646660","NCT07687082","Prevalence and Risk Factors for Chronic Post-Surgical Pain Following Video-Assisted Thoracic Surgery : The EVATHO Prospective Bicentric Cohort Study.","Study of the Prevalence of Chronic Postoperative Pain After Video-Assisted Thoracic Surgery: A Bicentric Cohort Study","EVATHO","Inclusion Criteria:\n\n* Adult patients undergoing video-assisted thoracic surgery (VATS) for thoracic surgery\n\nExclusion Criteria:\n\n* Age \\\u003C18 years\n* Adults under legal protection or unable to provide informed non-opposition\n* Patients unable to understand or complete the study questionnaires\n* Patients not affiliated with a French health insurance scheme.\n* Adults under legal protection, including judicial safeguard, guardianship, or curatorship.\n* Participation in another clinical study involving an ongoing exclusion period.\n* Pregnant or breastfeeding women.",true,"18 Years",{"count":86,"type":21},400,"OBSERVATIONAL","Chronic post-surgical pain (CPSP) remains a common complication after thoracic surgery and may significantly impair patients' quality of life. Although the widespread adoption of video-assisted thoracic surgery (VATS) has reduced surgical trauma and improved postoperative recovery, a substantial proportion of patients still develop persistent pain.\n\nThe EVATHO study is a multicenter prospective observational cohort designed to determine the prevalence of CPSP three months after VATS and to identify perioperative factors associated with its development. Adult patients undergoing thoracic surgery by VATS at Montpellier and Nice University Hospitals will be prospectively enrolled.\n\nPain intensity, neuropathic pain characteristics, anxiety, depression, quality of life, and analgesic consumption will be assessed using validated questionnaires during the perioperative period and at 1 and 3 months after surgery. The results of this study may help identify patients at increased risk of CPSP and improve perioperative pain management strategies following thoracic surgery.",[90,91,92,28],"Chronic Post-surgical Pain","Postoperative Pain After Thoracic Surgery","Neuropathic Pain","NOT_YET_RECRUITING","2026-06-29",{"date":96,"type":38},"2026-07-07",{"date":98,"type":21},"2026-08-01",{"date":100,"type":21},"2028-08-01",{"name":102,"class":45},"University Hospital, Montpellier",{"id":104,"slug":105,"hasResults":11,"nctId":106,"briefTitle":107,"officialTitle":108,"acronym":109,"eligibilityCriteria":110,"healthyVolunteers":11,"sex":16,"minAge":84,"maxAge":4,"enrollmentInfo":111,"targetDuration":4,"studyType":22,"phases":113,"briefSummary":114,"conditions":115,"keywords":120,"overallStatus":93,"whyStopped":4,"lastUpdateSubmitDate":124,"lastUpdatePostDateStruct":125,"startDateStruct":127,"completionDateStruct":129,"leadSponsor":131,"locationsCount":4},"100637194","impact-of-topical-aromatherapy-on-postoperative-quality-of-recovery-after-lung-resection-100637194","NCT07622602","Impact of Topical Aromatherapy on Postoperative Quality of Recovery After Lung Resection","Evaluation of the Impact of Aromatherapy Applied to the Skin as a Complementary Treatment on the Quality of Recovery (QoR) Following Lung Resection","AromaQoR","Inclusion Criteria:\n\n* Adults aged 18 years or older,\n* undergoing scheduled lung resection for diagnostic or therapeutic purposes\n* able to give free, informed, signed consent (no later than the day of inclusion and before any examination required by the research)\n* person affiliated with or beneficiary of a social security system.\n\nExclusion Criteria:\n\n* Patients with chronic pain prior to surgery\n* patients undergoing daily pain relief treatment prior to surgery\n* patients using essential oils applied to the skin for pain relief.\n* In relation to aromatherapy:\n* history of allergy to essential oils\n* atopic skin\n* known allergies\n* asthma\n* pregnant or breastfeeding women\n* nut allergies (in relation to sweet almond oil)\n* individuals who are vulnerable or deprived of their liberty by judicial or administrative decision\n* patients participating in other interventional studies on pain.",{"count":112,"type":21},124,[24],"The key to early surgery recovery lies in optimal and immediate control of postoperative pain. Despite standard pain management protocols, lung resection is often associated with acute, neuropathic, or chronic pain, compounded by the side effects of morphine-based treatments. In this context, aromatherapy can provide complementary support, both to alleviate pain and to improve the quality of recovery after surgery.",[28,116,117,118,119],"Postoperative Recovery","Pain","Complementary Therapies","Aromatherapy",[121,119,122,123],"Quality of Recovery","Essential Oil","Thoracic surgery","2026-05-27",{"date":126,"type":38},"2026-06-03",{"date":128,"type":21},"2026-06",{"date":130,"type":21},"2028-06",{"name":132,"class":45},"University Hospital, Toulouse"]