{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Catheter+Complications", "query": { "condition": "Catheter Complications" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 213, "total_pages": 22, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Catheter+Complications&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-05-22T04:51:23.600Z", "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": "NCT01068275", "title": "Lumbar Plexus Catheter Versus Femoral Nerve Catheter for Postoperative Pain After Anterior Cruciate Ligament (ACL) Repair", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Postoperative Pain" ], "interventions": [ { "name": "lumbar plexus catheter", "type": "PROCEDURE" }, { "name": "femoral nerve catheter", "type": "PROCEDURE" }, { "name": "single-shot femoral block", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Seattle Children's Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "11 Years", "maximum_age": "21 Years", "sex": "ALL", "summary": "11 Years to 21 Years" }, "enrollment_count": 114, "start_date": "2010-04", "completion_date": "2012-09", "has_results": false, "last_update_posted_date": "2010-08-26", "last_synced_at": "2026-05-22T04:51:23.600Z", "location_count": 1, "location_summary": "Seattle, Washington", "locations": [ { "city": "Seattle", "state": "Washington" } ], "official_url": "https://clinicaltrials.gov/study/NCT01068275" }, { "nct_id": "NCT01923129", "title": "Optimal Duration of Indwelling Urinary Catheter Following Pelvic Surgery", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Urinary Retention" ], "interventions": [ { "name": "Prazosin given 6 hours prior to catheter removal in the 24 hour group", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Cedars-Sinai Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 142, "start_date": "2012-11-30", "completion_date": "2017-11-22", "has_results": true, "last_update_posted_date": "2019-02-20", "last_synced_at": "2026-05-22T04:51:23.600Z", "location_count": 1, "location_summary": "Los Angeles, California", "locations": [ { "city": "Los Angeles", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT01923129" }, { "nct_id": "NCT03955653", "title": "Fluoroscopic-Guided Micropuncture Technique for Common Femoral Artery Access", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Catheter Related Complication" ], "interventions": [ { "name": "Femoral artey access", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "University of Alabama at Birmingham", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "90 Years", "sex": "ALL", "summary": "18 Years to 90 Years" }, "enrollment_count": 200, "start_date": "2019-04-30", "completion_date": "2019-10-30", "has_results": false, "last_update_posted_date": "2019-11-26", "last_synced_at": "2026-05-22T04:51:23.600Z", "location_count": 1, "location_summary": "Birmingham, Alabama", "locations": [ { "city": "Birmingham", "state": "Alabama" } ], "official_url": "https://clinicaltrials.gov/study/NCT03955653" }, { "nct_id": "NCT02210429", "title": "Supraclavicular Blocks for Post-Operative Pain Control in Supracondylar Fracture Fixation, a Retrospective Analysis of Single Shot Catheter Techniques", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Acute Pain", "Pain, Postoperative" ], "interventions": [ { "name": "Elbow Fracture Fixation", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Ann & Robert H Lurie Children's Hospital of Chicago", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": "17 Years", "sex": "ALL", "summary": "Up to 17 Years" }, "enrollment_count": 200, "start_date": "2009-01", "completion_date": "2015-11", "has_results": false, "last_update_posted_date": "2015-07-29", "last_synced_at": "2026-05-22T04:51:23.600Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT02210429" }, { "nct_id": "NCT01231204", "title": "Prevention of Post-Mastectomy Breast Pain Using Ambulatory Continuous Paravertebral Blocks", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Paravertebral Catheter Insertion", "Mastectomy", "Breast Cancer" ], "interventions": [ { "name": "Placebo (normal saline) Continuous Infusion", "type": "PROCEDURE" }, { "name": "Ropivicaine 0.4% Continuous Infusion", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "University of California, San Diego", "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": 60, "start_date": "2010-10", "completion_date": "2016-03", "has_results": false, "last_update_posted_date": "2016-04-11", "last_synced_at": "2026-05-22T04:51:23.600Z", "location_count": 1, "location_summary": "La Jolla, California", "locations": [ { "city": "La Jolla", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT01231204" }, { "nct_id": "NCT05906134", "title": "Minimally Invasive Esophagectomy Pain Control Trial", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1", "PHASE2" ], "conditions": [ "Postoperative Pain, Acute", "Postoperative Complications" ], "interventions": [ { "name": "Local intercostal nerve block", "type": "PROCEDURE" }, { "name": "Cryo-analgesia and intercostal nerve block", "type": "PROCEDURE" }, { "name": "Serratus plane catheter blocks and intercostal nerve blocks", "type": "PROCEDURE" }, { "name": "Thoracic epidural catheter", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Swedish Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 30, "start_date": "2022-04-26", "completion_date": "2027-02", "has_results": false, "last_update_posted_date": "2025-07-23", "last_synced_at": "2026-05-22T04:51:23.600Z", "location_count": 1, "location_summary": "Seattle, Washington", "locations": [ { "city": "Seattle", "state": "Washington" } ], "official_url": "https://clinicaltrials.gov/study/NCT05906134" }, { "nct_id": "NCT00876681", "title": "Ultrasound Guidance Versus Electrical Stimulation for Continuous Popliteal-Sciatic Nerve Blocks", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Postoperative Pain", "Foot Numbness" ], "interventions": [ { "name": "Popliteal catheter placed via ultrasound or electrical stimulation", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "University of California, San Diego", "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": "2008-04", "completion_date": "2009-04", "has_results": false, "last_update_posted_date": "2009-10-08", "last_synced_at": "2026-05-22T04:51:23.600Z", "location_count": 1, "location_summary": "San Diego, California", "locations": [ { "city": "San Diego", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT00876681" }, { "nct_id": "NCT04924569", "title": "Continence Care Registry", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Neurogenic Bladder", "Non-Neurogenic Bladder" ], "interventions": [], "intervention_types": [], "sponsor": "Hollister Incorporated", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 600, "start_date": "2021-05-24", "completion_date": "2030-05", "has_results": false, "last_update_posted_date": "2026-05-08", "last_synced_at": "2026-05-22T04:51:23.600Z", "location_count": 1, "location_summary": "Libertyville, Illinois", "locations": [ { "city": "Libertyville", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT04924569" }, { "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": "2026-05-22T04:51:23.600Z", "location_count": 1, "location_summary": "Cincinnati, Ohio", "locations": [ { "city": "Cincinnati", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT03127280" }, { "nct_id": "NCT03163394", "title": "HD5 Levels in Catheter Versus Bag Urine Specimens in Young Children for the Diagnosis of UTI", "overall_status": "TERMINATED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Urinary Tract Infections" ], "interventions": [], "intervention_types": [], "sponsor": "Le Bonheur Children's Hospital", "sponsor_class": "OTHER", "healthy_volunteers": null, "eligibility": { "minimum_age": "1 Month", "maximum_age": "24 Months", "sex": "ALL", "summary": "1 Month to 24 Months" }, "enrollment_count": 5, "start_date": "2017-04-23", "completion_date": "2019-06-10", "has_results": false, "last_update_posted_date": "2020-02-27", "last_synced_at": "2026-05-22T04:51:23.600Z", "location_count": 1, "location_summary": "Memphis, Tennessee", "locations": [ { "city": "Memphis", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT03163394" } ] }