[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Lu Chao\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":71},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,46],{"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":28,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100611037","transcutaneous-electrical-acupoint-stimulation-for-postoperative-urinary-retention-after-radical-surgery-for-cervical-cancer-100611037",false,"NCT07235371","Transcutaneous Electrical Acupoint Stimulation for Postoperative Urinary Retention After Radical Surgery for Cervical Cancer","Transcutaneous Electrical Acupoint Stimulation on Postoperative Urinary Retention After Radical Surgery for Cervical Cancer: A Randomized Controlled Trial","Inclusion Criteria:\n\n* (1) Age range of 18-70 years, expected survival period ≥ 6 months; (2) Meets diagnostic criteria, with an indwelling catheter duration of more than 14 days but less than 1 year; (3) No history of urinary system diseases before surgery; (4) Clear consciousness, unobstructed communication, daily living ability, patients or family members can learn TEAS operation; (5) No serious systemic diseases such as heart, liver, brain, kidney, etc; (6) Karnofsky functional status score (KPS) ≥ 70 points; (7) Voluntarily participate and sign a written informed consent form.\n\nExclusion Criteria:\n\n* (1) Obstructive urinary retention, such as urethral stricture or stones; (2) combined with other serious systemic diseases, advanced cachexia; (3) Patients with pacemaker implantation or metal implantation in the body; (4) The treatment site has skin lesions or is not suitable for TEAS treatment in other populations; (5) Physical or mental disorders with cognitive impairment; (6) Other clinical trial participants who are currently involved in affecting the results of this study; (7) Those who do not agree to participate in clinical trials; (8) The evaluator has determined that the participant is not suitable to participate in this study.","FEMALE","18 Years","70 Years",{"count":20,"type":21},76,"ESTIMATED","INTERVENTIONAL",[24],"NA","This is a prospective, blinded, single-center, randomized controlled trial. We will include 76 patients with postoperative urinary retention (POUR) after radical hysterectomy for cervical cancer who have a clear diagnosis and meet the screening criteria as the research object. They will be randomly divided into the transcutaneous electrical acupoint stimulation（TEAS）group and the sham TEAS group according to a 1:1 ratio. Each group consists of 38 patients, and all patients will be required to sign a written informed consent form. The TEAS group will be treated with TEAS based on conventional treatment, and the sham TEAS group will be treated with shamTEAS based on conventional treatment. The main outcomes will be the changes in post-void residual (PVR) volume; secondary indicators will include the response rate of participants with successful urinary catheter removal after intervention, assessment of urinary tract infection (UTI), and patient quality of life assessment according to the EORTC QLQ-C30 scale. The participants will also be evaluated with expectations, blind evaluation, compliance evaluation, and safety evaluation to preliminarily evaluate the effect of TEAS for postoperative urinary retention after radical hysterectomy for cervical cancer.",[27],"Postoperative Urinary Retention (POUR)",[29,30,31,32],"Postoperative urinary retention,","POUR","TEAS","transcutaneous electrical acupoint stimulation","RECRUITING","2026-02-05",{"date":36,"type":37},"2026-02-06","ACTUAL",{"date":39,"type":37},"2025-11-18",{"date":41,"type":21},"2028-11-30",{"name":43,"class":44},"Lu Chao","OTHER",1,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":4,"eligibilityCriteria":52,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":53,"targetDuration":4,"studyType":22,"phases":55,"briefSummary":56,"conditions":57,"keywords":58,"overallStatus":62,"whyStopped":4,"lastUpdateSubmitDate":63,"lastUpdatePostDateStruct":64,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":70,"locationsCount":4},"100612408","electroacupuncture-on-postoperative-urinary-retention-after-radical-surgery-for-cervical-cancer-100612408","NCT07253194","Electroacupuncture on Postoperative Urinary Retention After Radical Surgery for Cervical Cancer","Effect of Electroacupuncture on Postoperative Urinary Retention After Radical Surgery for Cervical Cancer： A Randomized Controlled Trial","Inclusion Criteria:\n\n* ① 18 to 70 years old;\n* ② Anticipated survival of at least 6 months;\n* ③ Met the diagnostic criteria for POUR of cervical cancer, and the duration of POUR is less than 6 months;\n* ④ No serious urinary system disease in the past, and no urinary retention before operation;\n* ⑤ Karnofsky functional status score (KPS) ≥ 70 points;\n* ⑥ Stable vital signs, no serious mental illness, capable of daily living, able to cooperate in completing all treatments and examinations;\n* ⑦ Voluntarily participate and sign a written informed consent form.\n\nExclusion Criteria:\n\n* ① Obstructive urinary retention, such as urethral stricture or stones induced urinary system diseases;\n* ② Merge other serious systemic diseases, and advanced cachexia patients;\n* ③ Patients who are intolerant to electrical stimulation therapy, such as those with pacemakers installed;\n* ④ With psychiatric disorder or severe cognitive impairment;\n* ⑤ Severe skin damage, infection, and ulceration at the treatment site;\n* ⑥ Those who are participating in other acupuncture or drug clinical trials.",{"count":54,"type":21},208,[24],"This is a prospective, blinded, single-center, randomized controlled trial. Investigators will include 208 patients with postoperative urinary retention (POUR) after radical hysterectomy for cervical cancer who have a clear diagnosis and meet the screening criteria. Participants will be randomly divided into the electroacupuncture（EA）group and the sham EA group according to a 1:1 ratio. Each group consists of 104 patients, and all participants will be required to sign a written informed consent form. The TEAS group will be treated with EA based on conventional treatment, and the shamEA group will be treated with sham EA based on conventional treatment. The main outcomes will be to calculate the proportion of patients who successfully removed the urinary catheter, and the secondary indicators will include the change in post-void residual (PVR) volume of the bladder, assessment of urinary tract infection (UTI), and quality of life assessment according to the EORTC QLQ-C30 scale. Evaluation of participant-reported expectations, blinding, compliance, and safety will also be conducted. All analyses will be conducted in accordance with the intention-to-treat principle.",[27],[59,30,60,61],"Postoperative urinary retention","Electroacupuncture","EA","NOT_YET_RECRUITING","2025-11-26",{"date":65,"type":37},"2025-11-28",{"date":67,"type":21},"2026-01-01",{"date":69,"type":21},"2028-12-31",{"name":43,"class":44},""]