{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Gynecologic+Infections", "query": { "condition": "Gynecologic Infections" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 10, "total_pages": 1, "next_page_url": null, "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-05-21T22:26:52.338Z", "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": "NCT03127280", "title": "Can Investigators Reduce Urinary Catheter Use and Lower Urinary Tract Infection Among Women Undergoing Benign Gynecologic Surgery?", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Urinary Tract Infections", "Urinary Retention", "Satisfaction" ], "interventions": [ { "name": "Fast Track foley removal", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "The Christ Hospital", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 200, "start_date": "2014-11-04", "completion_date": "2018-01-14", "has_results": false, "last_update_posted_date": "2018-01-30", "last_synced_at": "2026-05-21T22:26:52.338Z", "location_count": 1, "location_summary": "Cincinnati, Ohio", "locations": [ { "city": "Cincinnati", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT03127280" }, { "nct_id": "NCT01431326", "title": "Pharmacokinetics of Understudied Drugs Administered to Children Per Standard of Care", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Adenovirus", "Anesthesia", "Anxiety", "Anxiolysis", "Autism", "Autistic Disorder", "Bacterial Meningitis", "Bacterial Septicemia", "Benzodiazepine", "Bipolar Disorder", "Bone and Joint Infections", "Central Nervous System Infections", "Convulsions", "Cytomegalovirus Retinitis", "Early-onset Schizophrenia Spectrum Disorders", "Epilepsy", "General Anesthesia", "Gynecologic Infections", "Herpes Simplex Virus", "Infantile Hemangioma", "Infection", "Inflammation", "Inflammatory Conditions", "Intra-abdominal Infections", "Lower Respiratory Tract Infections", "Migraines", "Pain", "Pneumonia", "Schizophrenia", "Sedation", "Seizures", "Skeletal Muscle Spasms", "Skin and Skin-structure Infections", "Treatment-resistant Schizophrenia", "Urinary Tract Infections", "Withdrawal", "Sepsis", "Gram-negative Infection", "Bradycardia", "Cardiac Arrest", "Cardiac Arrhythmia", "Staphylococcal Infections", "Nosocomial Pneumonia", "Neuromuscular Blockade", "Methicillin Resistant Staphylococcus Aureus", "Endocarditis", "Neutropenia", "Headache", "Fibrinolytic Bleeding", "Pulmonary Arterial Hypertension", "CMV Retinitis", "Hypertension", "Chronic Kidney Diseases", "Hyperaldosteronism", "Hypokalemia", "Heart Failure", "Hemophilia", "Heavy Menstrual Bleeding", "Insomnia" ], "interventions": [ { "name": "The POPS study is collecting PK data on children prescribed the following drugs of interest per standard of care:", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Daniel Benjamin", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": "21 Years", "sex": "ALL", "summary": "Up to 21 Years" }, "enrollment_count": 3520, "start_date": "2011-11", "completion_date": "2019-11", "has_results": false, "last_update_posted_date": "2023-09-06", "last_synced_at": "2026-05-21T22:26:52.338Z", "location_count": 43, "location_summary": "Anchorage, Alaska • Little Rock, Arkansas • La Jolla, California + 37 more", "locations": [ { "city": "Anchorage", "state": "Alaska" }, { "city": "Little Rock", "state": "Arkansas" }, { "city": "La Jolla", "state": "California" }, { "city": "Los Angeles", "state": "California" }, { "city": "Los Angeles", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT01431326" }, { "nct_id": "NCT02071251", "title": "A Study to Evaluate a Quality Improvement Intervention to Reduce Wound Separation Rates in Obese Gynecologic Oncology Service Patients Undergoing Abdominal Surgery", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Wound Complications", "Wound Infection", "Wound Separation" ], "interventions": [ { "name": "Prospective wound complication protocol", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Washington University School of Medicine", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "89 Years", "sex": "FEMALE", "summary": "18 Years to 89 Years · Female only" }, "enrollment_count": 105, "start_date": "2011-12", "completion_date": "2013-07", "has_results": false, "last_update_posted_date": "2015-08-25", "last_synced_at": "2026-05-21T22:26:52.338Z", "location_count": 1, "location_summary": "St Louis, Missouri", "locations": [ { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT02071251" }, { "nct_id": "NCT01052038", "title": "Post Operative Sore Throat and Dexamethasone", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Sore Throat", "Pain" ], "interventions": [ { "name": "Placebo administration", "type": "DRUG" }, { "name": "Dexamethasone 0.05mg/kr administration", "type": "DRUG" }, { "name": "Dexamethasone 0.1mg/kg", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Northwestern University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "64 Years", "sex": "FEMALE", "summary": "18 Years to 64 Years · Female only" }, "enrollment_count": 120, "start_date": "2010-01", "completion_date": "2010-09", "has_results": true, "last_update_posted_date": "2012-05-02", "last_synced_at": "2026-05-21T22:26:52.338Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT01052038" }, { "nct_id": "NCT07234968", "title": "Clinical Trial to Evaluate Post-Operative Outcomes of Ureteral Stent vs Ureteral Stent Free Radical Cystectomy", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Bladder Cancer", "Muscle-Invasive Bladder Carcinoma", "Urothelial Carcinoma", "Pelvic Malignancy", "Bladder Transitional Cell Carcinoma", "Bladder Neoplasm" ], "interventions": [ { "name": "Ureteral Stent Placement", "type": "PROCEDURE" }, { "name": "No Ureteral Stent", "type": "PROCEDURE" }, { "name": "Indocyanine Green with Fluorescence Imaging", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "PROCEDURE", "DIAGNOSTIC_TEST" ], "sponsor": "Thomas Jefferson University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "85 Years", "sex": "ALL", "summary": "18 Years to 85 Years" }, "enrollment_count": 70, "start_date": "2025-12-23", "completion_date": "2028-04-30", "has_results": false, "last_update_posted_date": "2026-02-17", "last_synced_at": "2026-05-21T22:26:52.338Z", "location_count": 2, "location_summary": "Philadelphia, Pennsylvania", "locations": [ { "city": "Philadelphia", "state": "Pennsylvania" }, { "city": "Philadelphia", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT07234968" }, { "nct_id": "NCT01926756", "title": "Does Straight Catheterization in Short Gynecologic Procedures Cause Bacteriuria?", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Postoperative Bacteriuria" ], "interventions": [ { "name": "Straight catheterization", "type": "PROCEDURE" }, { "name": "No straight catheterization", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Abington Memorial Hospital", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 200, "start_date": "2013-07", "completion_date": null, "has_results": false, "last_update_posted_date": "2013-08-21", "last_synced_at": "2026-05-21T22:26:52.338Z", "location_count": 1, "location_summary": "Abington, Pennsylvania", "locations": [ { "city": "Abington", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT01926756" }, { "nct_id": "NCT05210556", "title": "Oral Antibiotic Bowel Preparation in Gynecologic Oncology Surgery", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Surgical Site Infection", "Surgical Complication", "Gynecologic Cancer" ], "interventions": [ { "name": "Diagnosed with Surgical Site Infection", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "WellSpan Health", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "99 Years", "sex": "FEMALE", "summary": "18 Years to 99 Years · Female only" }, "enrollment_count": 778, "start_date": "2021-12-22", "completion_date": "2024-06-30", "has_results": false, "last_update_posted_date": "2025-03-28", "last_synced_at": "2026-05-21T22:26:52.338Z", "location_count": 1, "location_summary": "York, Pennsylvania", "locations": [ { "city": "York", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT05210556" }, { "nct_id": "NCT06297187", "title": "Cavitronic Ultrasonic Surgical Aspiration (CUSA) Women's Health Study", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Vulvar Intraepithelial Neoplasia", "Condylomata Acuminata" ], "interventions": [ { "name": "CUSA (Cavitronic Ultrasonic Surgical Aspirator)", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Integra LifeSciences Corporation", "sponsor_class": "INDUSTRY", "healthy_volunteers": null, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 56, "start_date": "2024-02-23", "completion_date": "2024-08-31", "has_results": false, "last_update_posted_date": "2024-09-19", "last_synced_at": "2026-05-21T22:26:52.338Z", "location_count": 1, "location_summary": "Dallas, Texas", "locations": [ { "city": "Dallas", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT06297187" }, { "nct_id": "NCT04048356", "title": "Chlorhexidine vs. Iodine for Vaginal Preparation in Urogynecologic Procedures", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Pelvic Organ Prolapse", "Urinary Incontinence", "Pelvic Floor Disorders", "Gynecologic Disease", "Post-Op Infection", "Surgical Site Infection", "Urinary Tract Infections" ], "interventions": [ { "name": "Vaginal scrub, to be applied vaginally and perineally immediately prior to surgery.", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "University of New Mexico", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 137, "start_date": "2019-07-15", "completion_date": "2021-03-14", "has_results": true, "last_update_posted_date": "2023-07-10", "last_synced_at": "2026-05-21T22:26:52.338Z", "location_count": 1, "location_summary": "Albuquerque, New Mexico", "locations": [ { "city": "Albuquerque", "state": "New Mexico" } ], "official_url": "https://clinicaltrials.gov/study/NCT04048356" }, { "nct_id": "NCT01450800", "title": "Suppressive Therapy With Oral Antibiotics for Prevention of Postoperative Urinary Tract Infection (UTI)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Urinary Tract Infection" ], "interventions": [ { "name": "Nitrofurantoin", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Duke University", "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": 163, "start_date": "2011-08", "completion_date": "2013-09", "has_results": true, "last_update_posted_date": "2017-02-13", "last_synced_at": "2026-05-21T22:26:52.338Z", "location_count": 1, "location_summary": "Durham, North Carolina", "locations": [ { "city": "Durham", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT01450800" } ] }