{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=silk&page=2", "query": { "intervention": "silk", "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?intervention=silk&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-09-12T14:03:00.713Z", "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": "NCT04534660", "title": "Preliminary Safety and Effectiveness of SMI-01 as a Tissue Filler", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Nasolabial Fold", "Cheek Augmentation" ], "interventions": [ { "name": "SMI-01", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Sofregen Medical, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "22 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "22 Years to 65 Years" }, "enrollment_count": 21, "start_date": "2020-11-10", "completion_date": "2023-06-23", "has_results": false, "last_update_posted_date": "2024-05-31", "last_synced_at": "2026-09-12T14:03:00.713Z", "location_count": 2, "location_summary": "Encinitas, California • Miami, Florida", "locations": [ { "city": "Encinitas", "state": "California" }, { "city": "Miami", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT04534660" }, { "nct_id": "NCT01355666", "title": "Silk-Like Fabric for the Prevention of Pressure Sores in a Long Term Care Setting", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Pressure Ulcers" ], "interventions": [ { "name": "DermaTherapy® Linen and underpads.", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Precision Fabrics Group, Inc.", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 75, "start_date": "2010-09", "completion_date": "2011-06", "has_results": false, "last_update_posted_date": "2011-05-18", "last_synced_at": "2026-09-12T14:03:00.713Z", "location_count": 1, "location_summary": "Durham, North Carolina", "locations": [ { "city": "Durham", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT01355666" }, { "nct_id": "NCT03324997", "title": "Restylane Silk for Treatment of Chest Wrinkles", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Wrinkle" ], "interventions": [ { "name": "Restylane Silk", "type": "DRUG" }, { "name": "Saline", "type": "DRUG" }, { "name": "Optical Coherence Tomography", "type": "DEVICE" } ], "intervention_types": [ "DRUG", "DEVICE" ], "sponsor": "Heidi Waldorf", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "25 Years", "maximum_age": "55 Years", "sex": "FEMALE", "summary": "25 Years to 55 Years · Female only" }, "enrollment_count": 0, "start_date": "2018-01-28", "completion_date": "2018-01-28", "has_results": false, "last_update_posted_date": "2018-03-06", "last_synced_at": "2026-09-12T14:03:00.713Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT03324997" }, { "nct_id": "NCT02925741", "title": "Silk-Like Bed Linens for Prevention of Unit-Acquired Ulcers", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Pressure Ulcer" ], "interventions": [ { "name": "Silk-Like Linens", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "The Cleveland Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 3343, "start_date": "2014-03", "completion_date": "2015-03", "has_results": true, "last_update_posted_date": "2020-08-13", "last_synced_at": "2026-09-12T14:03:00.713Z", "location_count": 1, "location_summary": "Cleveland, Ohio", "locations": [ { "city": "Cleveland", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT02925741" }, { "nct_id": "NCT02519933", "title": "A Comparison of mNT-BBAVF and BCAVF in Hemodialysis Patients", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Vascular Fistula" ], "interventions": [ { "name": "mNT-BBAVF", "type": "PROCEDURE" }, { "name": "BCAVF", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Shanghai 10th People's Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "18 Years to 75 Years" }, "enrollment_count": 84, "start_date": "2016-04", "completion_date": "2019-08-31", "has_results": false, "last_update_posted_date": "2019-09-25", "last_synced_at": "2026-09-12T14:03:00.713Z", "location_count": 1, "location_summary": "Providence, Rhode Island", "locations": [ { "city": "Providence", "state": "Rhode Island" } ], "official_url": "https://clinicaltrials.gov/study/NCT02519933" }, { "nct_id": "NCT04458415", "title": "The Effect of Traxi Panniculus Retractor on Surgical Time at Non-emergent Cesarean Delivery in Obese Women", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Obesity" ], "interventions": [ { "name": "Traxi Panniculus Retractor (TPR)", "type": "OTHER" }, { "name": "Silk Tape", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Geisinger Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "FEMALE", "summary": "Female only" }, "enrollment_count": 0, "start_date": "2021-06-01", "completion_date": "2022-04-30", "has_results": false, "last_update_posted_date": "2021-08-11", "last_synced_at": "2026-09-12T14:03:00.713Z", "location_count": 1, "location_summary": "Danville, Pennsylvania", "locations": [ { "city": "Danville", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT04458415" }, { "nct_id": "NCT01559363", "title": "A Safety, Pharmacokinetic & Dose-Escalation Study of KD019 in Subjects With Autosomal Dominant Polycystic Kidney Disease", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1", "PHASE2" ], "conditions": [ "Polycystic Kidney, Autosomal Dominant" ], "interventions": [ { "name": "Tesevatinib", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Kadmon, a Sanofi Company", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "62 Years", "sex": "ALL", "summary": "18 Years to 62 Years" }, "enrollment_count": 69, "start_date": "2012-10-11", "completion_date": "2019-02-08", "has_results": true, "last_update_posted_date": "2022-11-08", "last_synced_at": "2026-09-12T14:03:00.713Z", "location_count": 11, "location_summary": "Los Angeles, California • Denver, Colorado • Kansas City, Kansas + 8 more", "locations": [ { "city": "Los Angeles", "state": "California" }, { "city": "Denver", "state": "Colorado" }, { "city": "Kansas City", "state": "Kansas" }, { "city": "Boston", "state": "Massachusetts" }, { "city": "Rochester", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT01559363" }, { "nct_id": "NCT05713253", "title": "A PHASED, PROSPECTIVE, MULTI-CENTER STUDY OF THE ELITA SYSTEM", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Refractive Error" ], "interventions": [ { "name": "ELITA System", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Johnson & Johnson Surgical Vision, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "22 Years", "maximum_age": null, "sex": "ALL", "summary": "22 Years and older" }, "enrollment_count": 96, "start_date": "2023-02-02", "completion_date": "2025-02-21", "has_results": false, "last_update_posted_date": "2026-03-16", "last_synced_at": "2026-09-12T14:03:00.713Z", "location_count": 2, "location_summary": "Palo Alto, California • Draper, Utah", "locations": [ { "city": "Palo Alto", "state": "California" }, { "city": "Draper", "state": "Utah" } ], "official_url": "https://clinicaltrials.gov/study/NCT05713253" }, { "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": "2026-09-12T14:03:00.713Z", "location_count": 1, "location_summary": "Corpus Christi, Texas", "locations": [ { "city": "Corpus Christi", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT06589284" }, { "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": "2026-09-12T14:03:00.713Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT01918059" } ] }