{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Restored&page=3", "query": { "intervention": "Restored", "page": 3 }, "page_size": 10 }, "pagination": { "page": 3, "page_size": 10, "total_count": 53, "total_pages": 6, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Restored&page=4&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Restored&page=2&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-21T08:02:47.708Z", "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": "NCT00782171", "title": "Evaluation of Immediate Versus Delayed Loading of Dental Implants With a Modified Surface", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Partial Edentulism" ], "interventions": [ { "name": "SLActive dental implant", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Institut Straumann AG", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 266, "start_date": "2004-07", "completion_date": "2010-02", "has_results": true, "last_update_posted_date": "2017-06-20", "last_synced_at": "2026-10-21T08:02:47.708Z", "location_count": 3, "location_summary": "Boca Raton, Florida • Indianapolis, Indiana • Philadelphia, Pennsylvania", "locations": [ { "city": "Boca Raton", "state": "Florida" }, { "city": "Indianapolis", "state": "Indiana" }, { "city": "Philadelphia", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT00782171" }, { "nct_id": "NCT03064126", "title": "RANGER™ Paclitaxel Coated Balloon vs Standard Balloon Angioplasty", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Peripheral Artery Disease", "Atherosclerosis", "Artery Diseases, Peripheral", "Plaque, Atherosclerotic", "Occlusive Arterial Disease" ], "interventions": [ { "name": "RANGER™ Paclitaxel Coated Balloon", "type": "DEVICE" }, { "name": "Paclitaxel", "type": "DRUG" }, { "name": "Standard Balloon Angioplasty", "type": "PROCEDURE" } ], "intervention_types": [ "DEVICE", "DRUG", "PROCEDURE" ], "sponsor": "Boston Scientific Corporation", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "20 Years", "maximum_age": null, "sex": "ALL", "summary": "20 Years and older" }, "enrollment_count": 440, "start_date": "2017-03-02", "completion_date": "2023-10-25", "has_results": true, "last_update_posted_date": "2024-10-29", "last_synced_at": "2026-10-21T08:02:47.708Z", "location_count": 42, "location_summary": "Fairhope, Alabama • Aurora, Colorado • Stratford, Connecticut + 38 more", "locations": [ { "city": "Fairhope", "state": "Alabama" }, { "city": "Aurora", "state": "Colorado" }, { "city": "Stratford", "state": "Connecticut" }, { "city": "Newark", "state": "Delaware" }, { "city": "Washington D.C.", "state": "District of Columbia" } ], "official_url": "https://clinicaltrials.gov/study/NCT03064126" }, { "nct_id": "NCT02440022", "title": "Study Comparing Lutonix AV Drug Coated Balloon vs Standard Balloon for Treatment of Dysfunctional AV Fistulae", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Arteriovenous Fistula" ], "interventions": [ { "name": "Lutonix DCB", "type": "COMBINATION_PRODUCT" }, { "name": "Standard Balloon Angioplasty Catheter", "type": "DEVICE" }, { "name": "Percutaneous Transluminal Angiography", "type": "PROCEDURE" } ], "intervention_types": [ "COMBINATION_PRODUCT", "DEVICE", "PROCEDURE" ], "sponsor": "C. R. Bard", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": null, "sex": "ALL", "summary": "21 Years and older" }, "enrollment_count": 285, "start_date": "2015-06", "completion_date": "2018-06", "has_results": true, "last_update_posted_date": "2020-05-06", "last_synced_at": "2026-10-21T08:02:47.708Z", "location_count": 23, "location_summary": "Birmingham, Alabama • Phoenix, Arizona • Tempe, Arizona + 20 more", "locations": [ { "city": "Birmingham", "state": "Alabama" }, { "city": "Phoenix", "state": "Arizona" }, { "city": "Tempe", "state": "Arizona" }, { "city": "Sacramento", "state": "California" }, { "city": "Newark", "state": "Delaware" } ], "official_url": "https://clinicaltrials.gov/study/NCT02440022" }, { "nct_id": "NCT03534141", "title": "Mild Hypothermia and Acute Kidney Injury in Liver Transplantation", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Cirrhosis", "End Stage Liver Disease", "Acute Kidney Injury", "Liver Transplant; Complications", "Chronic Kidney Diseases", "Hepatitis c", "Hepatitis B", "NASH - Nonalcoholic Steatohepatitis", "Alcoholic Cirrhosis", "Hepatocellular Carcinoma" ], "interventions": [ { "name": "Esophageal cooling/warming device", "type": "DEVICE" }, { "name": "Mild hypothermia", "type": "OTHER" }, { "name": "Normothermia", "type": "OTHER" } ], "intervention_types": [ "DEVICE", "OTHER" ], "sponsor": "University of California, San Francisco", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 175, "start_date": "2018-07-07", "completion_date": "2023-09-14", "has_results": true, "last_update_posted_date": "2025-05-16", "last_synced_at": "2026-10-21T08:02:47.708Z", "location_count": 3, "location_summary": "San Francisco, California • Aurora, Colorado • Houston, Texas", "locations": [ { "city": "San Francisco", "state": "California" }, { "city": "Aurora", "state": "Colorado" }, { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT03534141" }, { "nct_id": "NCT02698163", "title": "Nanodiamond Modified Gutta Percha (NDGP) Composite for Non-surgical Root Canal Therapy (RCT) Filler Material", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Dental Pulp Diseases", "Dental Pulp Necrosis", "Nerve Root Pain Nec" ], "interventions": [ { "name": "Nanodiamond reinforced Gutta Percha", "type": "DEVICE" }, { "name": "Gutta Percha", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of California, Los Angeles", "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": "2016-03", "completion_date": "2021-03", "has_results": true, "last_update_posted_date": "2022-01-21", "last_synced_at": "2026-10-21T08:02:47.708Z", "location_count": 1, "location_summary": "Los Angeles, California", "locations": [ { "city": "Los Angeles", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT02698163" }, { "nct_id": "NCT03712891", "title": "Evaluation of Providing Coffee to Patients Postoperatively to Decrease Length of Stay in the PACU", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "PACU Length of Stay", "Postoperative Nausea", "Postoperative Vomiting", "Patient Satisfaction" ], "interventions": [ { "name": "Coffee", "type": "DIETARY_SUPPLEMENT" } ], "intervention_types": [ "DIETARY_SUPPLEMENT" ], "sponsor": "TriHealth Inc.", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 178, "start_date": "2018-10-25", "completion_date": "2023-08-16", "has_results": true, "last_update_posted_date": "2024-12-13", "last_synced_at": "2026-10-21T08:02:47.708Z", "location_count": 1, "location_summary": "Cincinnati, Ohio", "locations": [ { "city": "Cincinnati", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT03712891" }, { "nct_id": "NCT02572570", "title": "Clinical Investigation of a New Bulk Fill Composite Resin in the Restoration of Posterior Teeth", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Dental Restoration Failure of Marginal Integrity", "Dental Caries", "Unrepairable Overhanging of Dental Restorative Materials", "Poor Aesthetics of Existing Restoration", "Secondary Dental Caries Associated With Failed or Defective Dental Restorations", "Fractured Dental Restorative Materials Without Loss of Materials", "Fracture of Dental Restorative Materials With Loss of Material" ], "interventions": [ { "name": "Filtek Bulk Fill Posterior", "type": "DEVICE" }, { "name": "Filtek Supreme Ultra", "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": "99 Years", "sex": "ALL", "summary": "18 Years to 99 Years" }, "enrollment_count": 27, "start_date": "2015-12", "completion_date": "2019-12-05", "has_results": true, "last_update_posted_date": "2020-12-19", "last_synced_at": "2026-10-21T08:02:47.708Z", "location_count": 1, "location_summary": "Chapel Hill, North Carolina", "locations": [ { "city": "Chapel Hill", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT02572570" }, { "nct_id": "NCT02546713", "title": "Abutment Macro Design and Peri-implant Tissues", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Edentulous" ], "interventions": [ { "name": "Abutment with concave subcritical contour", "type": "OTHER" }, { "name": "Abutment with convex subcritical contour", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Nova Southeastern University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": null, "sex": "ALL", "summary": "21 Years and older" }, "enrollment_count": 28, "start_date": "2015-12", "completion_date": "2021-11-30", "has_results": false, "last_update_posted_date": "2022-04-13", "last_synced_at": "2026-10-21T08:02:47.708Z", "location_count": 1, "location_summary": "Fort Lauderdale, Florida", "locations": [ { "city": "Fort Lauderdale", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT02546713" }, { "nct_id": "NCT00755469", "title": "Post-conditioning to Reduce Infarct Size", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Myocardial Infarction" ], "interventions": [ { "name": "Post-conditioning", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Minneapolis Heart Institute Foundation", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "18 Years to 80 Years" }, "enrollment_count": 43, "start_date": "2008-09", "completion_date": "2010-08", "has_results": false, "last_update_posted_date": "2013-12-05", "last_synced_at": "2026-10-21T08:02:47.708Z", "location_count": 1, "location_summary": "Minneapolis, Minnesota", "locations": [ { "city": "Minneapolis", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT00755469" }, { "nct_id": "NCT04845542", "title": "Promoting Resilience in Stroke Survivor-carepartner Dyads (ReStoreD)", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Stroke", "Depression, Anxiety", "Coping Skills", "Couples" ], "interventions": [ { "name": "ReStoreD", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Utah", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 400, "start_date": "2022-07-20", "completion_date": "2027-08-31", "has_results": false, "last_update_posted_date": "2026-01-30", "last_synced_at": "2026-10-21T08:02:47.708Z", "location_count": 1, "location_summary": "Salt Lake City, Utah", "locations": [ { "city": "Salt Lake City", "state": "Utah" } ], "official_url": "https://clinicaltrials.gov/study/NCT04845542" } ] }