{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=carbon+dioxide+lavage", "query": { "intervention": "carbon dioxide lavage" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 5, "total_pages": 1, "next_page_url": null, "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-09-20T03:19:27.347Z", "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": "NCT04818593", "title": "A Sibling Oocyte Study- Comparison of ZyMotTM Microfluidics Device to Density Gradient for Sperm Selection During ICSI", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "ART" ], "interventions": [ { "name": "ZyMot Multi Sperm Separation Device (850 ul)", "type": "DEVICE" }, { "name": "Density Gradient Centrifugation", "type": "OTHER" } ], "intervention_types": [ "DEVICE", "OTHER" ], "sponsor": "NYU Langone Health", "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": "2021-06-18", "completion_date": "2021-11-29", "has_results": true, "last_update_posted_date": "2023-06-05", "last_synced_at": "2026-09-20T03:19:27.347Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT04818593" }, { "nct_id": "NCT03882723", "title": "Noninvasive Ventilation Masks Carbon Dioxide Clearance in Normal Volunteers", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "CO2 Clearance", "Mask Comfort", "Rebreathing Exhaled Gas" ], "interventions": [ { "name": "Evaluated 4 masks used for NIV with mechanical ventilators", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Rush University 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": 8, "start_date": "2018-03-30", "completion_date": "2019-08-30", "has_results": true, "last_update_posted_date": "2023-06-28", "last_synced_at": "2026-09-20T03:19:27.347Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT03882723" }, { "nct_id": "NCT00736125", "title": "A Study to Determine if Carbon Dioxide Lavage During Total Knee Surgery Reduces Intraoperative Embolic Events", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Postoperative Complications", "Memory Disorders" ], "interventions": [ { "name": "pulsatile saline lavage", "type": "DEVICE" }, { "name": "carbon dioxide lavage", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Kinamed Incorporated", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "50 Years", "maximum_age": null, "sex": "ALL", "summary": "50 Years and older" }, "enrollment_count": 20, "start_date": "2007-12", "completion_date": "2011-03", "has_results": true, "last_update_posted_date": "2019-09-26", "last_synced_at": "2026-09-20T03:19:27.347Z", "location_count": 1, "location_summary": "Durham, North Carolina", "locations": [ { "city": "Durham", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT00736125" }, { "nct_id": "NCT06521502", "title": "The APS Phenotyping Study", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "ARDS", "Sepsis", "Pneumonia" ], "interventions": [ { "name": "Blood collection", "type": "OTHER" }, { "name": "Urine Collection", "type": "OTHER" }, { "name": "Nasal, oral, and rectal swabs", "type": "OTHER" }, { "name": "Stool collection", "type": "OTHER" }, { "name": "Heat Moisture Exchange Filter collection", "type": "OTHER" }, { "name": "Tracheal Aspirate sample collection", "type": "OTHER" }, { "name": "Non-bronchoscopic bronchoalveolar lavage (NBBAL)", "type": "PROCEDURE" }, { "name": "Surveys", "type": "OTHER" }, { "name": "Short physical performance battery", "type": "OTHER" }, { "name": "Hand grip strength", "type": "OTHER" }, { "name": "CNS Vital Signs", "type": "OTHER" }, { "name": "Muscle Ultrasound", "type": "OTHER" }, { "name": "Muscle Strength", "type": "OTHER" }, { "name": "Spirometry", "type": "OTHER" }, { "name": "Lung Diffusion Testing (DLCO)", "type": "OTHER" }, { "name": "Chest CT Scan", "type": "RADIATION" } ], "intervention_types": [ "OTHER", "PROCEDURE", "RADIATION" ], "sponsor": "Vanderbilt University 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": 4000, "start_date": "2024-07-25", "completion_date": "2029-04-30", "has_results": false, "last_update_posted_date": "2026-02-20", "last_synced_at": "2026-09-20T03:19:27.347Z", "location_count": 20, "location_summary": "Fresno, California • Palo Alto, California • San Francisco, California + 12 more", "locations": [ { "city": "Fresno", "state": "California" }, { "city": "Palo Alto", "state": "California" }, { "city": "San Francisco", "state": "California" }, { "city": "San Francisco", "state": "California" }, { "city": "Denver", "state": "Colorado" } ], "official_url": "https://clinicaltrials.gov/study/NCT06521502" }, { "nct_id": "NCT02004470", "title": "Lavage and Suction of the Right Upper Quadrant to Reduce Post Laparoscopic Shoulder Pain", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Shoulder Pain" ], "interventions": [ { "name": "Active lavage and suction", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "University of Tennessee", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "75 Years", "sex": "FEMALE", "summary": "18 Years to 75 Years · Female only" }, "enrollment_count": 100, "start_date": "2014-01", "completion_date": "2014-06", "has_results": false, "last_update_posted_date": "2014-01-06", "last_synced_at": "2026-09-20T03:19:27.347Z", "location_count": 4, "location_summary": "Chattanooga, Tennessee", "locations": [ { "city": "Chattanooga", "state": "Tennessee" }, { "city": "Chattanooga", "state": "Tennessee" }, { "city": "Chattanooga", "state": "Tennessee" }, { "city": "Chattanooga", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT02004470" } ] }