{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Adverse+Effects+Surgery&page=2", "query": { "condition": "Adverse Effects Surgery", "page": 2 }, "page_size": 10 }, "pagination": { "page": 2, "page_size": 10, "total_count": 10, "total_pages": 1, "next_page_url": null, "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Adverse+Effects+Surgery&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-06-11T01:26:23.381Z", "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": "NCT01707095", "title": "Bundling and Unbundling the Laparoscopic Electrosurgery Cord With the Camera Cord", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Fatigue" ], "interventions": [ { "name": "Unbundling of cords", "type": "OTHER" }, { "name": "Bundling of cords", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Colorado, Denver", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 84, "start_date": "2012-09", "completion_date": "2014-01", "has_results": true, "last_update_posted_date": "2014-07-17", "last_synced_at": "2026-06-11T01:26:23.381Z", "location_count": 1, "location_summary": "Aurora, Colorado", "locations": [ { "city": "Aurora", "state": "Colorado" } ], "official_url": "https://clinicaltrials.gov/study/NCT01707095" }, { "nct_id": "NCT04988490", "title": "Quantification of Cannabinoids and Comparison to Post-Surgical Pain Medication Requirements and Surgical Outcomes", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Post-Surgical Pain", "Post-Surgical Complication", "Cancer", "Cannabis Use" ], "interventions": [], "intervention_types": [], "sponsor": "University of Colorado, Denver", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 68, "start_date": "2021-10-11", "completion_date": "2024-06-14", "has_results": false, "last_update_posted_date": "2025-03-10", "last_synced_at": "2026-06-11T01:26:23.381Z", "location_count": 1, "location_summary": "Denver, Colorado", "locations": [ { "city": "Denver", "state": "Colorado" } ], "official_url": "https://clinicaltrials.gov/study/NCT04988490" }, { "nct_id": "NCT01280331", "title": "Comparison of the Safety of Q8003 Versus Morphine Equivalent Doses of Its Components (Oxycodone and Morphine) in Bunionectomy Patients", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Postoperative Pain" ], "interventions": [ { "name": "Q8003 (morphine sulfate and oxycodone hydrochloride)", "type": "DRUG" }, { "name": "Morphine sulfate", "type": "DRUG" }, { "name": "Oxycodone HCl", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "QRxPharma Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 375, "start_date": "2011-01", "completion_date": "2011-04", "has_results": false, "last_update_posted_date": "2012-05-17", "last_synced_at": "2026-06-11T01:26:23.381Z", "location_count": 4, "location_summary": "Anaheim, California • Owings Mills, Maryland • Pasadena, Maryland + 1 more", "locations": [ { "city": "Anaheim", "state": "California" }, { "city": "Owings Mills", "state": "Maryland" }, { "city": "Pasadena", "state": "Maryland" }, { "city": "San Antonio", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT01280331" }, { "nct_id": "NCT05221866", "title": "Efficiency And Quality In Post-Surgical Pain Therapy After Discharge", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Opioid Use", "Opioid Dependence", "Opioid Misuse", "Post-Surgical Complication" ], "interventions": [ { "name": "Empowering Patient to Steer Their Pain Management After Surgery", "type": "BEHAVIORAL" }, { "name": "Provider-facing Prescription Aid", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Nebraska", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "19 Years", "maximum_age": "89 Years", "sex": "ALL", "summary": "19 Years to 89 Years" }, "enrollment_count": 711, "start_date": "2022-05-02", "completion_date": "2023-12-10", "has_results": true, "last_update_posted_date": "2025-07-01", "last_synced_at": "2026-06-11T01:26:23.381Z", "location_count": 1, "location_summary": "Omaha, Nebraska", "locations": [ { "city": "Omaha", "state": "Nebraska" } ], "official_url": "https://clinicaltrials.gov/study/NCT05221866" }, { "nct_id": "NCT02958566", "title": "Multimodal Narcotic Limited Perioperative Pain Control With Colorectal Surgery", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Colon Cancer", "Colon Diverticulosis", "Colonic Neoplasms", "Colonic Diverticulitis", "Pain, Postoperative", "Ileus", "Ileus Paralytic", "Ileus; Mechanical", "Constipation Drug Induced", "Constipation", "Rectum Cancer", "Rectum Neoplasm" ], "interventions": [ { "name": "Acetaminophen", "type": "DRUG" }, { "name": "Gabapentin", "type": "DRUG" }, { "name": "Orphenadrine", "type": "DRUG" }, { "name": "Lidocaine", "type": "DRUG" }, { "name": "Marcaine", "type": "DRUG" }, { "name": "Ketamine", "type": "DRUG" }, { "name": "Methadone", "type": "DRUG" }, { "name": "Tramadol", "type": "DRUG" }, { "name": "Ketorolac", "type": "DRUG" }, { "name": "Morphine Sulfate", "type": "DRUG" }, { "name": "Fentanyl", "type": "DRUG" }, { "name": "Dilaudid", "type": "DRUG" }, { "name": "Hydrocodone-Acetaminophen Tab 5-325 MG", "type": "DRUG" }, { "name": "HYDROCODONE/ACETAMINOPHEN 5 Mg-325 Mg ORAL TABLET", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "University of Illinois College of Medicine at Peoria", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 80, "start_date": "2017-01", "completion_date": "2018-12", "has_results": false, "last_update_posted_date": "2017-03-20", "last_synced_at": "2026-06-11T01:26:23.381Z", "location_count": 1, "location_summary": "Peoria, Illinois", "locations": [ { "city": "Peoria", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT02958566" }, { "nct_id": "NCT06315582", "title": "Surgical Approach to Uterine Septum", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Uterine Septum", "Surgical Complication", "Septum; Uterus", "Treatment Side Effects", "Treatment" ], "interventions": [ { "name": "Removal of uterine septum with hysteroscopic scissors without electrosurgery.", "type": "PROCEDURE" }, { "name": "Hysteroscopic septoplasty utilizing bipolar electrosurgery", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Northwestern University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "22 Years", "maximum_age": "44 Years", "sex": "FEMALE", "summary": "22 Years to 44 Years · Female only" }, "enrollment_count": 40, "start_date": "2024-03-11", "completion_date": "2026-12", "has_results": false, "last_update_posted_date": "2026-06-01", "last_synced_at": "2026-06-11T01:26:23.381Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT06315582" }, { "nct_id": "NCT04324359", "title": "Study to See How Well an Eye Drop, SURF-201, Works and What Side Effects There Are in Cataract Surgery Subjects", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Post-surgical Ocular Inflammation", "Post-surgical Ocular Pain" ], "interventions": [ { "name": "SURF-201", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Surface Ophthalmics, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 91, "start_date": "2020-03-03", "completion_date": "2020-11-20", "has_results": true, "last_update_posted_date": "2025-01-15", "last_synced_at": "2026-06-11T01:26:23.381Z", "location_count": 10, "location_summary": "Hemet, California • Murrieta, California • Brooksville, Florida + 7 more", "locations": [ { "city": "Hemet", "state": "California" }, { "city": "Murrieta", "state": "California" }, { "city": "Brooksville", "state": "Florida" }, { "city": "Jacksonville", "state": "Florida" }, { "city": "Stuart", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT04324359" }, { "nct_id": "NCT00748267", "title": "Hypnosis in Reducing Pain and Other Side Effects in Women Undergoing Surgery for Breast Cancer", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Anxiety Disorder", "Breast Cancer", "Nausea and Vomiting", "Pain" ], "interventions": [ { "name": "questionnaire administration", "type": "OTHER" }, { "name": "hypnotherapy", "type": "PROCEDURE" }, { "name": "therapeutic conventional surgery", "type": "PROCEDURE" } ], "intervention_types": [ "OTHER", "PROCEDURE" ], "sponsor": "City of Hope Medical Center", "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": 20, "start_date": "2008-08", "completion_date": "2010-12", "has_results": false, "last_update_posted_date": "2011-03-07", "last_synced_at": "2026-06-11T01:26:23.381Z", "location_count": 1, "location_summary": "Duarte, California", "locations": [ { "city": "Duarte", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT00748267" }, { "nct_id": "NCT06649890", "title": "A Novel Surgical Irrigation Solution in Post-Mastectomy Reconstruction: Evaluating Xperience™", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Surgical Site Infection", "Surgical Complication", "Implant Infection", "Implant Complication" ], "interventions": [ { "name": "Xperience™ Advanced Surgical Irrigation", "type": "DEVICE" }, { "name": "Dilute Povidone-Iodine", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of North Carolina, Chapel Hill", "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": 224, "start_date": "2025-06-30", "completion_date": "2028-06-30", "has_results": false, "last_update_posted_date": "2025-08-07", "last_synced_at": "2026-06-11T01:26:23.381Z", "location_count": 1, "location_summary": "Chapel Hill, North Carolina", "locations": [ { "city": "Chapel Hill", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT06649890" }, { "nct_id": "NCT00724750", "title": "Comparison of Two Methods of Negative Pressure Wound Therapy", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Acute Wounds From Trauma", "Dehiscence or Surgical Complications" ], "interventions": [ { "name": "Gauze suction (G-SUC)", "type": "DEVICE" }, { "name": "Vacuum Assisted Closure Device (VAC)", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of Chicago", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 87, "start_date": "2006-07", "completion_date": "2008-05", "has_results": true, "last_update_posted_date": "2015-10-19", "last_synced_at": "2026-06-11T01:26:23.381Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT00724750" } ] }