[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"postoperative-pain-relief\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:postoperative-pain-relief":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,44],{"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":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":5},"100644606","pbm-patch-for-postoperative-pain-relief-after-urological-surgery-100644606",false,"NCT07671612","PBM Patch for Postoperative Pain Relief After Urological Surgery","A Double-blind Randomized Controlled Clinical Study of the PBM Patch for Postoperative Pain Relief After Urological Surgery","Inclusion Criteria:\n\n1. Patients aged 18 years or older undergoing unilateral nephroureterectomy with bladder cuff excision, or adrenalectomy (tumor size \\\u003C 3.5 cm).\n2. Patients who are capable of clear verbal communication.\n3. Patients who are able to provide written informed consent.\n\nExclusion Criteria:\n\n1. Individuals with photosensitive constitution or those currently using photosensitizing medications.\n2. Individuals with a known history of severe allergy or contact dermatitis to medical adhesive patches or tapes.\n3. Patients with severe psychiatric illness or cognitive impairment.\n4. Long-term or high-dose opioid users.\n5. Patients utilizing a Patient-Controlled Analgesia (PCA) pump.\n6. Individuals with severe hepatic insufficiency or active liver disease.\n7. Vulnerable populations, individuals with restricted legal capacity, or those who are unable or unwilling to undergo clinical evaluations.","ALL","18 Years",{"count":19,"type":20},300,"ESTIMATED","INTERVENTIONAL",[23],"NA","This study is a prospective, randomized, double-blind, placebo-controlled clinical study designed to evaluate the efficacy and safety of a photobiomodulation (PBM) patch (Super Vi PBM Patch - Soothing) and an enhanced PBM patch (Super Vi PBM Patch - Soothing EX), compared with a placebo patch, for postoperative pain relief following urological surgery, including nephroureterectomy with bladder cuff resection (NU+BCR) and adrenalectomy (ADRX).",[26,27,28,29,30],"Urological Surgery","Photobiomodulation (PBM)","Non-pharmacological Intervention","Double-blind Randomized Controlled Study","Postoperative Pain Relief",[30,27,26,29,28],"NOT_YET_RECRUITING","2026-06-25",{"date":35,"type":36},"2026-06-26","ACTUAL",{"date":38,"type":20},"2026-07-01",{"date":40,"type":20},"2028-03-31",{"name":42,"class":43},"National Taiwan University Hospital","OTHER",{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":49,"acronym":50,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":52,"enrollmentInfo":53,"targetDuration":4,"studyType":55,"phases":4,"briefSummary":56,"conditions":57,"keywords":58,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":71},"100578520","bilateral-thorathic-erector-spinae-plane-block-in-laparoscopic-bariatic-surgeries-100578520","NCT06812364","Bilateral Thorathic Erector Spinae Plane Block in Laparoscopic Bariatic Surgeries","COMPARISON OF THE EFFICACY OF ONE LEVEL AND TWO LEVEL OF BILATERAL THORACIC ERECTOR SPINAE PLANE BLOCK COMBINED WITH GENERAL ANESTHESIA IN LAPAROSCOPIC BARIATRIC SURGERY FOR OBESE PATIENTS: RANDOMIZED CONTROLLED TRIAL","ESPBbariatrics","Inclusion Criteria:\n\n* Patient age ranges 18 to 60 years old\n* Obese patients ; Body mass index(BMI) ≥ 35 - 50 kg\u002Fm2\n* American Society of Anesthesiologists (13) physical status classes II to III\n* Patients scheduled for laparoscopic bariatric surgery i.e. sleeve gastrectomy and\u002For Roux-en-Y gastric bypass (RYGB) surgeries\n\nExclusion Criteria:\n\n* • Refusal of regional block\n\n  * Patients with neurological, psychological disorders or those lacking cooperation.\n  * Patients scheduled for concomitant laparoscopic cholecystectomy or paraumbilical hernia repair or those with history of previous bariatric surgery or obstructive sleep apnea.\n  * Patients with anatomic abnormalities at site of injection, skin lesions or wounds at site of proposed needle insertion.\n  * Patients with bleeding disorders defined as (INR \\>1.4) and\u002F or (platelet count \\\u003C100,000\u002FµL)\n  * Patients with hepatic disease e.g. liver cell failure or hepatic malignancy or hepatic enlargement.\n  * Patients who are allergic to amide local anesthetics","60 Years",{"count":54,"type":20},58,"OBSERVATIONAL","The study is to evaluate effectiveness of one-level versus two-level thoracic ESP block on intraoperative and postoperative analgesia in bariatric surgeries and to compare total opioid consumption of both groups.",[30],[59,60,61],"one level ESPB","two level ESPB","bariatric surgery","2025-02-01",{"date":64,"type":36},"2025-02-06",{"date":66,"type":20},"2025-03-01",{"date":68,"type":20},"2025-10-20",{"name":70,"class":43},"Cairo University",1]