[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"gynecology\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:gynecology":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,45,85,128,152],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":17,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":29,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100545950","acupuncture-for-chronic-pelvic-pain-100545950",false,"NCT06388590","Acupuncture for Chronic Pelvic Pain","\\*\\*Patients must be able to get care at Nellis Air Force Base (a military installation) in order to participate in this study\\*\\*\n\nInclusion Criteria:\n\n* Active Duty and DoD Female Beneficiaries (i.e. former military, spouse, dependent) aged 21-65 with chronic pelvic pain\n* Have negative laparoscopic findings for endometriosis\n\nExclusion Criteria:\n\n* Severe mental health disorders to include any disorder with psychotic features (e.g schizophrenia, bipolar, schizoaffective disorder)\n* Pelvic pain as a result of severe physical trauma (excluding sexual assault) such as traumatic childbirth, pelvic fractures or any other trauma as determined by the PI or AI.\n* Pregnancy","FEMALE","21 Years","65 Years",{"count":19,"type":20},64,"ESTIMATED","INTERVENTIONAL",[23],"NA","The objective of this study is to determine if alternative pain management strategies, namely acupuncture, may help reduce intensity of female pelvic pain compared to other pain control modalities. This research study will focus specifically on the Dragon's protocol of acupuncture which will seek to alleviate chronic non-endometriosis pelvic pain for women both with and without a history of sexual assault.\n\nThis study may support evidence for an inexpensive alternative means of treatment for patients with or without traumatic sexual history and chronic pelvic pain.",[26,27,28],"Pelvic Pain","Acupuncture","Gynecology",[30,31],"integrative medicine","acupuncture","RECRUITING","2026-04-09",{"date":35,"type":36},"2026-04-14","ACTUAL",{"date":38,"type":36},"2024-12-01",{"date":40,"type":20},"2026-10",{"name":42,"class":43},"David Moss","FED",1,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":4,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":52,"minAge":53,"maxAge":4,"enrollmentInfo":54,"targetDuration":4,"studyType":21,"phases":56,"briefSummary":57,"conditions":58,"keywords":65,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":75,"lastUpdatePostDateStruct":76,"startDateStruct":78,"completionDateStruct":79,"leadSponsor":81,"locationsCount":84},"100561028","enhanced-vitals-monitoring-after-major-surgery-trial-100561028","NCT06584825","Enhanced Vitals Monitoring After Major Surgery Trial","The Impact of Enhanced Postoperative Vitals Monitoring In-hospital and at Home vs. Standard Care After Inpatient Abdominal and Vascular Surgery: A Pilot Two-centre Randomized Controlled Study","Inclusion Criteria:\n\n1. Undergoing inpatient major abdominal (general surgery, urology, or gynecology) or vascular surgery at St. Paul's Hospital (SPH) and Mount Saint Joseph (MSJ) Hospital\n2. Length of stay of at least 48 hours (planned by the clinical team, or by the Canadian Institute of Health Information Discharge Abstract Database Expected Length of Stay (ELOS) for the surgical case mix group\n3. Self-reported fluency in reading and speaking in English for patient or home caregiver\n4. Living within British Columbia, Canada and in an area that is covered by Bell cellular network (the Cloud DX Inc. device has cellular Long Term Evolution (LTE) using the Bell network).\n\nExclusion Criteria:\n\n1. Patient refusal\n2. Transplant surgery, since these patients have a unique set of considerations and postoperative course.\n3. Inability to communicate with research personnel, perform self-monitoring of vital signs, or complete study surveys due to cognitive, language, visual, or hearing barriers\n4. Lack of capacity to consent to the study (including under the active influence of sedative medication or having received general anesthetic within the past 24 hours)\n5. Unable to use (or does not have a caregiver who can help put on\u002Ftake off) study monitoring device at home\n6. Preoperatively known planned discharge to a nursing home or rehabilitation facility\n7. Patient with known allergic reactions to any part material of the device\n8. Unable to monitor blood pressure accurately noninvasively using arm blood pressure cuffs, such as due to underlying vascular anatomy or non-pulsatile blood flow physiology\n9. Unlikely to be able to return the home monitoring kit (no fixed address, living too far away from site, etc.)","ALL","19 Years",{"count":55,"type":20},110,[23],"The aim of this clinical trial is to examine the feasibility of an enhanced vital sign monitoring solution in-hospital and at-home. This study includes adult patients undergoing inpatient major vascular or abdominal surgery. Researchers will compare the enhanced vitals monitoring group to the standard of care group to see if it may change post-operative management and outcomes. The primary question it aims to answer is if enhanced monitoring of surgical patient vitals can increase the number of days at home alive in the first 30 days after surgery. Participants in the intervention group will test two vitals monitoring devices, one in the hospital and one at home. They will also be asked to complete several questionnaires and a follow up phone call.",[59,60,61,62,63,64,28],"Surgery","Post Operative Complications","Quality of Recovery","General Surgery","Vascular Surgery","Urology",[66,67,68,69,70,71,72,73,74],"Days alive and at home","DAH30","Quality of Recovery 15","Pilot Randomized Controlled Trial","vitals","blood pressure","heart rate","oxygen saturation","device","2025-11-17",{"date":77,"type":36},"2025-11-21",{"date":75,"type":36},{"date":80,"type":20},"2027-12-31",{"name":82,"class":83},"University of British Columbia","OTHER",2,{"id":86,"slug":87,"hasResults":11,"nctId":88,"briefTitle":89,"officialTitle":90,"acronym":4,"eligibilityCriteria":91,"healthyVolunteers":11,"sex":15,"minAge":92,"maxAge":17,"enrollmentInfo":93,"targetDuration":4,"studyType":21,"phases":95,"briefSummary":96,"conditions":97,"keywords":107,"overallStatus":118,"whyStopped":4,"lastUpdateSubmitDate":119,"lastUpdatePostDateStruct":120,"startDateStruct":122,"completionDateStruct":124,"leadSponsor":126,"locationsCount":44},"100603856","yoga-in-women-with-surgical-menopause-after-gynecological-cancer-100603856","NCT07141953","Yoga in Women With Surgical Menopause After Gynecological Cancer","The Effect of Yoga on Quality of Life, Sleep Quality, and Spiritual Well-Being in Women Who Undergo Surgical Menopause Following Gynecological Cancer Surgery: A Randomized Controlled Trial","Inclusion Criteria:\n\nAge between 18-65 years Diagnosis of primary gynecological cancer (ovarian, endometrial, cervical, vaginal, or vulvar) (Stage I-III) Ability to read, understand, and speak Turkish Completion of all adjuvant treatments (surgery, chemotherapy, and\u002For radiotherapy) at least 6 months prior Access to the internet Having a computer\u002Ftablet\u002Fphone with a camera Willingness and ability to attend at least 80% of the yoga sessions Voluntary participation in the study\n\nExclusion Criteria:\n\nAny condition that prevents communication Cognitive, sensory, or physical impairment that prevents yoga practice Diagnosis of metastatic gynecological cancer Regular yoga practice within the last 6 months (at least once a week for 8 consecutive weeks)","18 Years",{"count":94,"type":20},46,[23],"This randomized controlled trial investigates the effects of yoga on quality of life, sleep quality, and spiritual well-being in women who have entered surgical menopause after gynecological cancer surgery. Yoga is expected to be a supportive intervention for symptom management and to improve overall well-being in this patient population.",[98,28,99,100,101,102,103,104,105,106],"Gynecological Oncology","Oncology","Surgical Menopause","Symptom Management","Quality of Life","Sleep Quality","Well-being","Yoga","Yoga for Cancer",[108,109,110,111,112,113,114,115,116,117],"gynecological oncology","gynecology","oncology","surgical menopause","symptom management","quality of life","sleep quality","well-being","yoga","yoga for cancer","NOT_YET_RECRUITING","2025-08-19",{"date":121,"type":36},"2025-08-26",{"date":123,"type":20},"2025-09-01",{"date":125,"type":20},"2026-06-01",{"name":127,"class":83},"Dokuz Eylul University",{"id":129,"slug":130,"hasResults":11,"nctId":131,"briefTitle":132,"officialTitle":133,"acronym":4,"eligibilityCriteria":134,"healthyVolunteers":135,"sex":52,"minAge":4,"maxAge":4,"enrollmentInfo":136,"targetDuration":4,"studyType":21,"phases":138,"briefSummary":139,"conditions":140,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":143,"lastUpdatePostDateStruct":144,"startDateStruct":146,"completionDateStruct":148,"leadSponsor":150,"locationsCount":44},"100593430","surgical-operating-room-enhancement-curriculum-for-medical-students-100593430","NCT07006337","Surgical Operating Room Enhancement Curriculum for Medical Students","Surgical Operating Room Enhancement Curriculum for Medical Students: A Quality Improvement and Prospective Cohort Study","Inclusion Criteria:\n\n* Medical students currently enrolled in the Wayne State University OBGYN clinical rotation (5-week block)\n* Willingness to voluntarily participate in surveys and training sessions\n* Ability to attend all didactic lectures\n\nExclusion Criteria:\n\n* Prior completion of a structured surgical operating room enrichment course (e.g., elective subspecialty training)\n* Inability to participate virtual sessions due to conflicting clinical\u002Facademic schedules\n* Non-English speakers (due to English-language survey instruments)",true,{"count":137,"type":20},60,[23],"The goal of this clinical trial is to assess whether integrating an enhanced Surgical Operating Room (OR) curriculum into the medical student program improves knowledge and proficiency in gynecologic surgical techniques and procedures among medical students at Wayne State University. The main questions it aims to answer are:\n\nDoes the Surgical Operating Room Enrichment Course increase medical students' knowledge and comfort with gynecologic surgical procedures?\n\nDoes participation in the course improve students' clinical perceptions and management of gynecologic emergencies?\n\nResearchers will compare students who participate in the Surgical Operating Room Enrichment Course (intervention group) to those who complete the standard rotation (control group) to see if the enhanced curriculum leads to greater improvements in knowledge and clinical skills.\n\nParticipants will:\n\nAttend virtual didactic lectures covering gynecologic anatomy, perioperative care, surgical techniques, and management of gynecologic emergencies\n\nComplete pre- and post-training surveys assessing knowledge, skills, and perceptions related to gynecologic surgery\n\nThis study involves approximately 60 medical students, with participation being voluntary and all responses de-identified.",[28,141,142],"Medical Education","Operating Rooms","2025-05-27",{"date":145,"type":36},"2025-06-05",{"date":147,"type":36},"2025-05-15",{"date":149,"type":20},"2026-09-01",{"name":151,"class":83},"Wayne State University",{"id":153,"slug":154,"hasResults":11,"nctId":155,"briefTitle":156,"officialTitle":157,"acronym":4,"eligibilityCriteria":158,"healthyVolunteers":11,"sex":15,"minAge":92,"maxAge":4,"enrollmentInfo":159,"targetDuration":4,"studyType":21,"phases":161,"briefSummary":162,"conditions":163,"keywords":165,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":169,"lastUpdatePostDateStruct":170,"startDateStruct":172,"completionDateStruct":174,"leadSponsor":176,"locationsCount":84},"100565474","evaluation-and-comparison-between-general-anesthesia-vs-two-types-of-combined-anesthesia-for-opioid-consumption-in-laparoscopic-hysterectomy-100565474","NCT06642649","Evaluation and Comparison Between General Anesthesia VS Two Types of Combined Anesthesia for Opioid Consumption in Laparoscopic Hysterectomy","Evaluation and Comparison Between General Anesthesia VS Two Types of Combined Anesthesia (general and Spinal Anesthesia) for Opioid Consumption in Laparoscopic Hysterectomy: a Multi-Center, Randomized, Prospective, Controlled Trial","Inclusion Criteria:\n\n* patients over 18 year of age,\n* ASA physical status I to III scheduled for laparoscopic hysterectomy (with or without adnexectomy)\n\nExclusion Criteria:\n\n* patients with inability to consent,\n* patient refusal,\n* contraindication to spinal anesthesia (e.g., hemodynamic instability, infection at the surgery site, and neurologic defects such as transverse myelitis, coagulopathies or ongoing anticoagulant therapy),\n* known chronic pain syndrome, known\n* suspected non- compliance,\n* drug, or alcohol abuse ,\n* major oncological surgeries,\n* allergy to drugs used in the protocol,\n* previous chronic use of analgesics\n* history of opioid abuse",{"count":160,"type":20},45,[23],"The aim of the study is to evaluate and compare general anesthesia VS two types of combined anesthesia in opioid consumption after laparoscopic hysterectomy",[164,28],"Laparoscopic Hysterectomy",[166,167,168],"laparoscopic hysterectomy","spinal anesthesia","general anesthesia","2025-02-26",{"date":171,"type":36},"2025-02-28",{"date":173,"type":36},"2024-11-01",{"date":175,"type":20},"2026-04-30",{"name":177,"class":83},"Andrea Saporito"]