{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=2-Octyl+cyanoacrylate&page=2", "query": { "intervention": "2-Octyl cyanoacrylate", "page": 2 }, "page_size": 10 }, "pagination": { "page": 2, "page_size": 10, "total_count": 35, "total_pages": 4, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=2-Octyl+cyanoacrylate&page=3&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=2-Octyl+cyanoacrylate&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-09-30T17:04:09.928Z", "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": "NCT02838017", "title": "Tissue Adhesive vs. Sterile Strips After Cesarean Delivery", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Wound Complication", "Complications; Cesarean Section" ], "interventions": [ { "name": "Tissue Adhesive", "type": "DEVICE" }, { "name": "Sterile strips", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Endeavor Health", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "FEMALE", "summary": "Female only" }, "enrollment_count": 504, "start_date": "2016-11", "completion_date": "2018-06", "has_results": true, "last_update_posted_date": "2019-08-14", "last_synced_at": "2026-09-30T17:04:09.928Z", "location_count": 3, "location_summary": "Chicago, Illinois • Evanston, Illinois • Highland Park, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" }, { "city": "Evanston", "state": "Illinois" }, { "city": "Highland Park", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT02838017" }, { "nct_id": "NCT03891004", "title": "Skin Closure With Tissue Adhesives vs. Subcuticular Suture After Robotic Urogynecologic Procedures", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Surgical Wound", "Tissue Adhesion" ], "interventions": [ { "name": "Subcuticular Skin Closure", "type": "PROCEDURE" }, { "name": "Tissue Adhesives", "type": "DEVICE" } ], "intervention_types": [ "PROCEDURE", "DEVICE" ], "sponsor": "St. John Hospital & Medical Center", "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": 47, "start_date": "2018-03-20", "completion_date": "2018-12-31", "has_results": false, "last_update_posted_date": "2019-04-04", "last_synced_at": "2026-09-30T17:04:09.928Z", "location_count": 1, "location_summary": "Detroit, Michigan", "locations": [ { "city": "Detroit", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT03891004" }, { "nct_id": "NCT03899753", "title": "Closure After Total Shoulder Arthroplasty: Prineo vs Dermabond", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Shoulder Arthritis", "Shoulder Arthropathy Associated With Other Conditions" ], "interventions": [ { "name": "2-Octyl Cyanoacrylate and Mesh", "type": "DEVICE" }, { "name": "2-Octyl Cyanoacrylate", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Montefiore Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "100 Years", "sex": "ALL", "summary": "18 Years to 100 Years" }, "enrollment_count": 1, "start_date": "2020-12-31", "completion_date": "2021-04-21", "has_results": true, "last_update_posted_date": "2023-07-03", "last_synced_at": "2026-09-30T17:04:09.928Z", "location_count": 1, "location_summary": "The Bronx, New York", "locations": [ { "city": "The Bronx", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT03899753" }, { "nct_id": "NCT01591603", "title": "Comparison of Perineural Catheter Depth for the Continuous Popliteal Nerve Block Using Ultrasound Guidance and Dermabond", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Neuromuscular Inhibition" ], "interventions": [ { "name": "1 cm", "type": "PROCEDURE" }, { "name": "5 cm", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Vanderbilt University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 83, "start_date": "2012-05", "completion_date": "2015-07", "has_results": false, "last_update_posted_date": "2015-07-20", "last_synced_at": "2026-09-30T17:04:09.928Z", "location_count": 1, "location_summary": "Nashville, Tennessee", "locations": [ { "city": "Nashville", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT01591603" }, { "nct_id": "NCT05278013", "title": "Utility of 2- Octyl Cyanoacrylate (2-OCA)", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Ascites", "Fluid Loss" ], "interventions": [ { "name": "Dermabond", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Methodist Health System", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "100 Years", "sex": "ALL", "summary": "18 Years to 100 Years" }, "enrollment_count": 134, "start_date": "2022-01-13", "completion_date": "2024-01-13", "has_results": false, "last_update_posted_date": "2023-07-10", "last_synced_at": "2026-09-30T17:04:09.928Z", "location_count": 1, "location_summary": "Dallas, Texas", "locations": [ { "city": "Dallas", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT05278013" }, { "nct_id": "NCT02037659", "title": "Dermabond Treatment for Gastric Variceal Bleeding", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Gastric Varices" ], "interventions": [ { "name": "DermaBond treatment of Gastric Varices", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Indiana University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 98, "start_date": "2012-12", "completion_date": "2022-03", "has_results": false, "last_update_posted_date": "2022-03-29", "last_synced_at": "2026-09-30T17:04:09.928Z", "location_count": 1, "location_summary": "Indianapolis, Indiana", "locations": [ { "city": "Indianapolis", "state": "Indiana" } ], "official_url": "https://clinicaltrials.gov/study/NCT02037659" }, { "nct_id": "NCT01918059", "title": "Cosmetic Outcome Study of Lid Laceration Repair With Suture Versus Tissue Adhesive", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Eyelid Laceration" ], "interventions": [ { "name": "Tissue Adhesive skin closure", "type": "PROCEDURE" }, { "name": "Absorbable suture skin closure", "type": "PROCEDURE" }, { "name": "Non-absorbable suture skin closure", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "The University of Texas Health Science Center, Houston", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 4, "start_date": "2013-08", "completion_date": "2014-11", "has_results": false, "last_update_posted_date": "2014-12-03", "last_synced_at": "2026-09-30T17:04:09.928Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT01918059" }, { "nct_id": "NCT00890578", "title": "HISTOACRYL: A Study of Its Efficacy in Final Scar Formation", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Surgical Incisions" ], "interventions": [ { "name": "adhesive to suture", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Mayo Clinic", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "21 Years", "maximum_age": null, "sex": "FEMALE", "summary": "21 Years and older · Female only" }, "enrollment_count": 21, "start_date": "2009-04", "completion_date": "2011-02", "has_results": false, "last_update_posted_date": "2012-06-21", "last_synced_at": "2026-09-30T17:04:09.928Z", "location_count": 1, "location_summary": "Jacksonville, Florida", "locations": [ { "city": "Jacksonville", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT00890578" }, { "nct_id": "NCT06589284", "title": "Skin Glue Versus Suture for Securing Radial Arterial Lines", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Arterial Catheters", "Catheter Related Complication" ], "interventions": [ { "name": "Silk 0-0 suture covered by chlorhexidine gluconate dressing", "type": "PROCEDURE" }, { "name": "2-octyl cyanoacrylate covered by chlorhexidine gluconate dressing", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "CHRISTUS Health", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 70, "start_date": "2023-06-15", "completion_date": "2024-06-14", "has_results": false, "last_update_posted_date": "2024-09-19", "last_synced_at": "2026-09-30T17:04:09.928Z", "location_count": 1, "location_summary": "Corpus Christi, Texas", "locations": [ { "city": "Corpus Christi", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT06589284" }, { "nct_id": "NCT07613892", "title": "Post Operative Skin Approximation With Cyanoacrylate Based Wound Closure Adhesives", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Wound Closure", "Dehisced Surgical Wounds" ], "interventions": [ { "name": "Evaluating wound closure products to close larger surgical site incisions", "type": "DEVICE" }, { "name": "Evaluating wound closure products to close smaller surgical site incisions", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Medline Industries", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 60, "start_date": "2025-04-02", "completion_date": "2026-03-18", "has_results": false, "last_update_posted_date": "2026-05-29", "last_synced_at": "2026-09-30T17:04:09.928Z", "location_count": 1, "location_summary": "Johnstown, Colorado", "locations": [ { "city": "Johnstown", "state": "Colorado" } ], "official_url": "https://clinicaltrials.gov/study/NCT07613892" } ] }