{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Hysterectomy&page=5", "query": { "condition": "Hysterectomy", "page": 5 }, "page_size": 10 }, "pagination": { "page": 5, "page_size": 10, "total_count": 210, "total_pages": 21, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Hysterectomy&page=6&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Hysterectomy&page=4&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-20T17:44:12.156Z", "attribution": "Data derived from public ClinicalTrials.gov records. The official record at https://clinicaltrials.gov/ remains the source of truth for current availability, contacts, and full study details.", "notes": [ "This endpoint exposes only public summary fields — no participant contact emails, phone numbers, or scraped investigator contact details.", "For contact information and full protocol detail, follow each trial's `official_url` to the ClinicalTrials.gov record.", "This API is a navigational aid. It does not provide medical advice, eligibility determinations, or compensation guarantees." ], "trials": [ { "nct_id": "NCT04797585", "title": "Vaginal Hysterectomy vs Supracervical Hysterectomy at the Time of Sacrocolpopexy", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Vaginal Hysterectomy", "Laparoscopic Supracervical Hysterectomy" ], "interventions": [ { "name": "Laparoscopic supracervical hysterectomy", "type": "OTHER" }, { "name": "Vaginal hysterectomy", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "The Cleveland Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 3, "start_date": "2021-03-16", "completion_date": "2023-09-12", "has_results": true, "last_update_posted_date": "2024-09-19", "last_synced_at": "2026-10-20T17:44:12.156Z", "location_count": 1, "location_summary": "Cleveland, Ohio", "locations": [ { "city": "Cleveland", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT04797585" }, { "nct_id": "NCT01814579", "title": "Vaginal Cuff Closure Time Using Unidirectional Barbed Suture in Robotic Hysterectomy", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Disease (or Disorder); Gynecological" ], "interventions": [ { "name": "Unidirectional Barbed Suture (V-Loc)", "type": "DEVICE" }, { "name": "polyglactin 910 (Vicryl)", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of Tennessee", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 80, "start_date": "2012-07", "completion_date": "2013-08", "has_results": false, "last_update_posted_date": "2013-03-26", "last_synced_at": "2026-10-20T17:44:12.156Z", "location_count": 2, "location_summary": "Memphis, Tennessee", "locations": [ { "city": "Memphis", "state": "Tennessee" }, { "city": "Memphis", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT01814579" }, { "nct_id": "NCT06671639", "title": "Stanford Program to Accelerate Robotic Children's Surgery", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Sleeve Gastrectomy", "Cholecystectomy", "Splenectomy", "Hysterectomy", "Endometriosis", "Ureteral Re-implant", "Cervical and Thoracic Tracheoplasty", "Thymectomy", "Lobectomy/Wedge Lung Resection", "Lung Segmentectomy", "Bronchoplasty", "Endoscopic Laryngeal/Pharyngeal Suturing", "Vocal Feminization", "Laryngeal Cleft Repair", "Endolaryngeal Adjacent Tissue Transfer", "Pharyngoplasty", "Ileocolonic Resections", "Laryngoplasty", "Proctectomy With Ileal Pouch-Anal Anastomosis" ], "interventions": [ { "name": "da Vinci Xi Robotic Surgery System", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Stanford University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "6 Years", "maximum_age": "21 Years", "sex": "ALL", "summary": "6 Years to 21 Years" }, "enrollment_count": 250, "start_date": "2025-08-01", "completion_date": "2028-02-28", "has_results": false, "last_update_posted_date": "2026-04-30", "last_synced_at": "2026-10-20T17:44:12.156Z", "location_count": 1, "location_summary": "Stanford, California", "locations": [ { "city": "Stanford", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT06671639" }, { "nct_id": "NCT00002536", "title": "Surgery With or Without Chemotherapy in Treating Patients With Stage IB Cervical Cancer", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Cervical Cancer" ], "interventions": [ { "name": "cisplatin", "type": "DRUG" }, { "name": "vincristine sulfate", "type": "DRUG" }, { "name": "surgical procedure", "type": "PROCEDURE" }, { "name": "radiation therapy", "type": "RADIATION" } ], "intervention_types": [ "DRUG", "PROCEDURE", "RADIATION" ], "sponsor": "Gynecologic Oncology Group", "sponsor_class": "NETWORK", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "FEMALE", "summary": "Female only" }, "enrollment_count": null, "start_date": "1996-12", "completion_date": null, "has_results": false, "last_update_posted_date": "2013-07-09", "last_synced_at": "2026-10-20T17:44:12.156Z", "location_count": 41, "location_summary": "Birmingham, Alabama • Bellflower, California • Los Angeles, California + 35 more", "locations": [ { "city": "Birmingham", "state": "Alabama" }, { "city": "Bellflower", "state": "California" }, { "city": "Los Angeles", "state": "California" }, { "city": "Los Gatos", "state": "California" }, { "city": "Orange", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT00002536" }, { "nct_id": "NCT03627234", "title": "Same Day Discharge vs. Overnight Stay After Hysterectomy", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Satisfaction", "Safety Issues", "Quality of Life" ], "interventions": [ { "name": "Same Day Discharge", "type": "BEHAVIORAL" }, { "name": "Overnight Stay", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "George Washington University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "FEMALE", "summary": "18 Years to 65 Years · Female only" }, "enrollment_count": 0, "start_date": "2018-07-10", "completion_date": "2021-09-08", "has_results": false, "last_update_posted_date": "2022-10-13", "last_synced_at": "2026-10-20T17:44:12.156Z", "location_count": 1, "location_summary": "Washington D.C., District of Columbia", "locations": [ { "city": "Washington D.C.", "state": "District of Columbia" } ], "official_url": "https://clinicaltrials.gov/study/NCT03627234" }, { "nct_id": "NCT00579787", "title": "Prospective Study Assessing Emotional, Sexual and Quality of Life Concerns Of Women Undergoing Removal of the Cervix Versus Removal of the Uterus,Ovaries and Fallopian Tubes For Treatment Of Early Stage Cervical Cancer", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Cervical Cancer" ], "interventions": [], "intervention_types": [], "sponsor": "Memorial Sloan Kettering Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "45 Years", "sex": "FEMALE", "summary": "18 Years to 45 Years · Female only" }, "enrollment_count": 72, "start_date": "2004-01", "completion_date": "2010-11", "has_results": false, "last_update_posted_date": "2010-12-02", "last_synced_at": "2026-10-20T17:44:12.156Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT00579787" }, { "nct_id": "NCT05480111", "title": "The Role of Quadratus Lumborum Blocks Following Minimally Invasive Hysterectomy", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Pain, Postoperative" ], "interventions": [ { "name": "Local anesthesia at incision site", "type": "DRUG" }, { "name": "Sham QL", "type": "DRUG" }, { "name": "Sham Local", "type": "DRUG" }, { "name": "QL", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "The University of Texas Health Science Center, Houston", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 76, "start_date": "2022-09-07", "completion_date": "2023-04-07", "has_results": true, "last_update_posted_date": "2024-06-05", "last_synced_at": "2026-10-20T17:44:12.156Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT05480111" }, { "nct_id": "NCT04318340", "title": "A Novel Tapered Applicator for Vaginal Vault Brachytherapy", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Endometrial Cancer", "Brachytherapy", "Quality of Life" ], "interventions": [ { "name": "Tapered applicator", "type": "OTHER" }, { "name": "Standard applicator", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Yale University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 21, "start_date": "2020-07-16", "completion_date": "2023-03-20", "has_results": false, "last_update_posted_date": "2023-07-14", "last_synced_at": "2026-10-20T17:44:12.156Z", "location_count": 1, "location_summary": "New Haven, Connecticut", "locations": [ { "city": "New Haven", "state": "Connecticut" } ], "official_url": "https://clinicaltrials.gov/study/NCT04318340" }, { "nct_id": "NCT00746018", "title": "Thermal Spread Into the Interstitial Portion of the Fallopian Tubes Using the Ligasure Device at Time of Hysterectomy", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Cervical Cancer", "Ovarian Cancer", "Uterine Cancer" ], "interventions": [ { "name": "LigaSure vessel sealing system", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Memorial Sloan Kettering Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": null, "sex": "FEMALE", "summary": "21 Years and older · Female only" }, "enrollment_count": 39, "start_date": "2008-08", "completion_date": "2017-07", "has_results": true, "last_update_posted_date": "2018-04-11", "last_synced_at": "2026-10-20T17:44:12.156Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT00746018" }, { "nct_id": "NCT00359866", "title": "Pelvic IMRT With Tomotherapy: A Phase I Feasibility Study in Post-Hysterectomy Cervical Cancer Patients", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Uterine Cervical Neoplasms" ], "interventions": [ { "name": "IMRT with tomotherapy", "type": "RADIATION" } ], "intervention_types": [ "RADIATION" ], "sponsor": "Washington University School of Medicine", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 28, "start_date": "2006-02", "completion_date": "2016-01", "has_results": false, "last_update_posted_date": "2016-06-15", "last_synced_at": "2026-10-20T17:44:12.156Z", "location_count": 1, "location_summary": "St Louis, Missouri", "locations": [ { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT00359866" } ] }