{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Preoperative+Care", "query": { "condition": "Preoperative Care" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 34, "total_pages": 4, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Preoperative+Care&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-06-10T22:14:46.995Z", "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": "NCT01857349", "title": "Efficacy of Surgical Preparation Solutions in Knee Surgery", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Arthroplasty, Replacement" ], "interventions": [ { "name": "Chlora Prep", "type": "OTHER" }, { "name": "Dura Prep", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Texas Tech University Health Sciences Center", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "89 Years", "sex": "ALL", "summary": "18 Years to 89 Years" }, "enrollment_count": 77, "start_date": "2013-04", "completion_date": "2020-07-20", "has_results": false, "last_update_posted_date": "2020-10-20", "last_synced_at": "2026-06-10T22:14:46.995Z", "location_count": 1, "location_summary": "Lubbock, Texas", "locations": [ { "city": "Lubbock", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT01857349" }, { "nct_id": "NCT06003985", "title": "Gastric Ultrasound Assessment for Patients Taking GLP1 Agonists", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Gastric Ultrasound", "Glucagon-like Peptide 1", "Point of Care Ultrasound" ], "interventions": [ { "name": "Gastric Ultrasound Exam", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Hospital for Special Surgery, New York", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "99 Years", "sex": "ALL", "summary": "18 Years to 99 Years" }, "enrollment_count": 354, "start_date": "2023-08-29", "completion_date": "2025-02-01", "has_results": false, "last_update_posted_date": "2025-11-26", "last_synced_at": "2026-06-10T22:14:46.995Z", "location_count": 7, "location_summary": "Washington D.C., District of Columbia • Jacksonville, Florida • Albany, New York + 2 more", "locations": [ { "city": "Washington D.C.", "state": "District of Columbia" }, { "city": "Jacksonville", "state": "Florida" }, { "city": "Albany", "state": "New York" }, { "city": "New York", "state": "New York" }, { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT06003985" }, { "nct_id": "NCT01676051", "title": "Surgical Prep in Hand Surgery", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Surgical Scrubbing", "Disinfection" ], "interventions": [ { "name": "Skin culture", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Pittsburgh", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "89 Years", "sex": "ALL", "summary": "18 Years to 89 Years" }, "enrollment_count": 240, "start_date": "2012-12", "completion_date": "2017-10", "has_results": false, "last_update_posted_date": "2017-10-31", "last_synced_at": "2026-06-10T22:14:46.995Z", "location_count": 2, "location_summary": "Pittsburgh, Pennsylvania", "locations": [ { "city": "Pittsburgh", "state": "Pennsylvania" }, { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT01676051" }, { "nct_id": "NCT05086406", "title": "Virtual and Video Counseling Versus In-Office Counseling for Laparoscopic Hysterectomy", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Patient Engagement" ], "interventions": [ { "name": "Combination of Video and Virtual Pre-operative Counseling", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "The Cleveland Clinic", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "20 Years", "maximum_age": null, "sex": "FEMALE", "summary": "20 Years and older · Female only" }, "enrollment_count": 128, "start_date": "2021-05-01", "completion_date": "2025-12", "has_results": false, "last_update_posted_date": "2025-02-19", "last_synced_at": "2026-06-10T22:14:46.995Z", "location_count": 1, "location_summary": "Weston, Florida", "locations": [ { "city": "Weston", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT05086406" }, { "nct_id": "NCT01456585", "title": "Phase 1 Study of Preoperative Gemcitabine Plus CP-870, 893 Followed by Addition of CP-870,893 to Standard -Of-care Adjuvant Chemoradiation for Patients With Newly Diagnosed Resectable Pancreatic Carcinoma", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Adenocarcinoma Pancreas" ], "interventions": [ { "name": "Gemcitabine", "type": "OTHER" }, { "name": "CP-870,893", "type": "DRUG" } ], "intervention_types": [ "OTHER", "DRUG" ], "sponsor": "Abramson Cancer Center at Penn Medicine", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 10, "start_date": "2012-04", "completion_date": "2013-04", "has_results": false, "last_update_posted_date": "2018-08-27", "last_synced_at": "2026-06-10T22:14:46.995Z", "location_count": 1, "location_summary": "Philadelphia, Pennsylvania", "locations": [ { "city": "Philadelphia", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT01456585" }, { "nct_id": "NCT04498208", "title": "Immune Modulation by Enhanced vs Standard Prehabilitation Program Before Major Surgery", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Surgery", "Immune System and Related Disorders", "Preoperative Care", "Gastrointestinal Disease", "Urological Disease", "Gynecologic Disease", "Thoracic Diseases" ], "interventions": [ { "name": "Physical Prehabilitation", "type": "BEHAVIORAL" }, { "name": "Stress Reduction Prehabilitation", "type": "BEHAVIORAL" }, { "name": "Cognitive Prehabilitation", "type": "BEHAVIORAL" }, { "name": "Nutrition Prehabilitation", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Stanford University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 55, "start_date": "2020-10-07", "completion_date": "2024-04-21", "has_results": false, "last_update_posted_date": "2024-04-23", "last_synced_at": "2026-06-10T22:14:46.995Z", "location_count": 1, "location_summary": "Stanford, California", "locations": [ { "city": "Stanford", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT04498208" }, { "nct_id": "NCT01184196", "title": "ChloraPrep Versus Betadine for Elective Knee Replacement Surgery", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Arthroplasty, Knee Replacement", "Replacement, Total Knee", "Total Knee Replacement" ], "interventions": [ { "name": "Swab area with Betadine", "type": "DRUG" }, { "name": "Swab area with ChloraPrep", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Central DuPage Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 55, "start_date": "2009-11", "completion_date": "2012-12", "has_results": false, "last_update_posted_date": "2013-04-16", "last_synced_at": "2026-06-10T22:14:46.995Z", "location_count": 1, "location_summary": "Winfield, Illinois", "locations": [ { "city": "Winfield", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT01184196" }, { "nct_id": "NCT06038734", "title": "Using Point-of-Care-Ultrasound (POCUS) to Assess Gastric Contents Among Fasting Pre-operative Patients Taking GLP-1 Agonists.", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Delayed Gastric Emptying", "Gastroparesis" ], "interventions": [ { "name": "gastric ultrasound", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "DIAGNOSTIC_TEST" ], "sponsor": "University of North Carolina, Chapel Hill", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 108, "start_date": "2023-11-10", "completion_date": "2024-04-17", "has_results": false, "last_update_posted_date": "2024-06-27", "last_synced_at": "2026-06-10T22:14:46.995Z", "location_count": 1, "location_summary": "Chapel Hill, North Carolina", "locations": [ { "city": "Chapel Hill", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT06038734" }, { "nct_id": "NCT06054282", "title": "A Mobile Application for Child-focused Perioperative Education", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Preoperative Anxiety" ], "interventions": [ { "name": "\"Ready for Tonsillectomy\" educational mobile application", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Children's Healthcare of Atlanta", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "5 Years", "maximum_age": "13 Years", "sex": "ALL", "summary": "5 Years to 13 Years" }, "enrollment_count": 360, "start_date": "2024-02-19", "completion_date": "2024-06", "has_results": false, "last_update_posted_date": "2024-02-22", "last_synced_at": "2026-06-10T22:14:46.995Z", "location_count": 1, "location_summary": "Atlanta, Georgia", "locations": [ { "city": "Atlanta", "state": "Georgia" } ], "official_url": "https://clinicaltrials.gov/study/NCT06054282" }, { "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": "2026-06-10T22:14:46.995Z", "location_count": 1, "location_summary": "Albuquerque, New Mexico", "locations": [ { "city": "Albuquerque", "state": "New Mexico" } ], "official_url": "https://clinicaltrials.gov/study/NCT04048356" } ] }