{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Reconstructive+Surgery&page=12", "query": { "intervention": "Reconstructive Surgery", "page": 12 }, "page_size": 10 }, "pagination": { "page": 12, "page_size": 10, "total_count": 909, "total_pages": 91, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Reconstructive+Surgery&page=13&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Reconstructive+Surgery&page=11&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-23T15:21:27.338Z", "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": "NCT01447277", "title": "Prospective Femoral Versus Femoral and Sciatic Nerve Block for Anterior Cruciate Ligament (ACL) Reconstruction", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Anterior Cruciate Ligament Tear" ], "interventions": [ { "name": "Sciatic Block", "type": "PROCEDURE" }, { "name": "Femoral Block only", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "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": 68, "start_date": "2011-10", "completion_date": "2013-06", "has_results": false, "last_update_posted_date": "2020-02-21", "last_synced_at": "2026-10-23T15:21:27.338Z", "location_count": 1, "location_summary": "San Francisco, California", "locations": [ { "city": "San Francisco", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT01447277" }, { "nct_id": "NCT00618358", "title": "Vascular Sealant Study", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Arteriovenous Access Grafts or Extra-anatomic and Infra-inguinal Grafts" ], "interventions": [ { "name": "Vascular Sealant System", "type": "DEVICE" }, { "name": "Gelfoam/Thrombin", "type": "OTHER" } ], "intervention_types": [ "DEVICE", "OTHER" ], "sponsor": "Georgetown University", "sponsor_class": "OTHER", "healthy_volunteers": null, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": null, "start_date": "2007-03", "completion_date": null, "has_results": false, "last_update_posted_date": "2015-03-27", "last_synced_at": "2026-10-23T15:21:27.338Z", "location_count": 1, "location_summary": "Washington D.C., District of Columbia", "locations": [ { "city": "Washington D.C.", "state": "District of Columbia" } ], "official_url": "https://clinicaltrials.gov/study/NCT00618358" }, { "nct_id": "NCT02917421", "title": "Accelerated Radiation Therapy (ART) to the Breast and Nodal Stations", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1", "PHASE2" ], "conditions": [ "Breast Cancer" ], "interventions": [ { "name": "Radiation", "type": "RADIATION" } ], "intervention_types": [ "RADIATION" ], "sponsor": "Weill Medical College of Cornell University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "19 Years", "maximum_age": "99 Years", "sex": "FEMALE", "summary": "19 Years to 99 Years · Female only" }, "enrollment_count": 88, "start_date": "2016-12-19", "completion_date": "2026-12-31", "has_results": true, "last_update_posted_date": "2026-04-17", "last_synced_at": "2026-10-23T15:21:27.338Z", "location_count": 3, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" }, { "city": "New York", "state": "New York" }, { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT02917421" }, { "nct_id": "NCT02228889", "title": "RCT of Two Noncrosslinked Porcine Acellular Dermal Matrices in Ab Wall Reconstruction", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Hernia, Ventral", "Intestinal Fistula", "Fibromatosis, Abdominal" ], "interventions": [ { "name": "Abdominal wall reconstruction with Strattice", "type": "PROCEDURE" }, { "name": "Assess pain intensity at last office visit preoperatively", "type": "OTHER" }, { "name": "Assess pain interference at last office visit preoperatively", "type": "OTHER" }, { "name": "Assess physical functioning at last office visit preoperatively", "type": "OTHER" }, { "name": "Assess patient quality of life at last office visit preoperatively", "type": "OTHER" }, { "name": "Assess patient pain intensity postoperatively", "type": "OTHER" }, { "name": "Assess pain interference postoperatively", "type": "OTHER" }, { "name": "Assess physical functioning postoperatively", "type": "OTHER" }, { "name": "Assess quality of life postoperatively", "type": "OTHER" }, { "name": "Assess hernia recurrence at 30 days postoperatively", "type": "OTHER" }, { "name": "Assess bulge at 30 days postoperatively", "type": "OTHER" }, { "name": "Assess Surgical Site Occurrences at 30 days postoperatively", "type": "OTHER" }, { "name": "Assess hernia recurrence at 1 year postoperatively", "type": "OTHER" }, { "name": "Assess bulge at 1 year postoperatively", "type": "OTHER" }, { "name": "Assess Surgical Site Occurrences at 1 year postoperatively", "type": "OTHER" }, { "name": "Assess overall complications at 30 days postoperatively", "type": "OTHER" }, { "name": "Assess overall complications at 1 year postoperatively", "type": "OTHER" }, { "name": "Abdominal wall reconstruction with XenMatrix", "type": "PROCEDURE" }, { "name": "Strattice", "type": "DEVICE" }, { "name": "XenMatrix", "type": "DEVICE" } ], "intervention_types": [ "PROCEDURE", "OTHER", "DEVICE" ], "sponsor": "Jeffrey Janis", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "99 Years", "sex": "ALL", "summary": "18 Years to 99 Years" }, "enrollment_count": 46, "start_date": "2015-01", "completion_date": "2025-03-27", "has_results": true, "last_update_posted_date": "2025-06-06", "last_synced_at": "2026-10-23T15:21:27.338Z", "location_count": 1, "location_summary": "Columbus, Ohio", "locations": [ { "city": "Columbus", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT02228889" }, { "nct_id": "NCT04692831", "title": "Testing a New Imaging Agent to Identify Cancer", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "HER-2 Positive Malignant Carcinoma of Breast", "HER-2 Protein Overexpression", "HER2-positive Metastatic Breast Cancer" ], "interventions": [ { "name": "89Zr-ss-pertuzumab PET/CT", "type": "COMBINATION_PRODUCT" } ], "intervention_types": [ "COMBINATION_PRODUCT" ], "sponsor": "Memorial Sloan Kettering Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 60, "start_date": "2020-11-30", "completion_date": "2027-11-30", "has_results": false, "last_update_posted_date": "2026-07-13", "last_synced_at": "2026-10-23T15:21:27.338Z", "location_count": 7, "location_summary": "Basking Ridge, New Jersey • Middletown, New Jersey • Montvale, New Jersey + 4 more", "locations": [ { "city": "Basking Ridge", "state": "New Jersey" }, { "city": "Middletown", "state": "New Jersey" }, { "city": "Montvale", "state": "New Jersey" }, { "city": "Commack", "state": "New York" }, { "city": "Harrison", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT04692831" }, { "nct_id": "NCT03678467", "title": "Evaluation of EpiBone-CMF for Mandibular Ramus Reconstruction", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1", "PHASE2" ], "conditions": [ "Mandible Tumor", "Mandibular Injuries", "Mandible; Deformity" ], "interventions": [ { "name": "EB-CMF", "type": "COMBINATION_PRODUCT" } ], "intervention_types": [ "COMBINATION_PRODUCT" ], "sponsor": "Epibone, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "18 Years to 65 Years" }, "enrollment_count": 6, "start_date": "2021-03-31", "completion_date": "2023-11", "has_results": false, "last_update_posted_date": "2022-05-27", "last_synced_at": "2026-10-23T15:21:27.338Z", "location_count": 3, "location_summary": "San Francisco, California • Cleveland, Ohio • San Antonio, Texas", "locations": [ { "city": "San Francisco", "state": "California" }, { "city": "Cleveland", "state": "Ohio" }, { "city": "San Antonio", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT03678467" }, { "nct_id": "NCT01273909", "title": "Outcomes After Perforator Flap Reconstruction for Breast Reconstruction and/or Lymphedema Treatment", "overall_status": "UNKNOWN", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Breast Cancer", "Hereditary Breast/Ovarian Cancer (brca1, brca2)", "Acquired Lymphedema", "Congenital Lymphedema" ], "interventions": [ { "name": "Perforator Flap Breast Reconstruction", "type": "PROCEDURE" }, { "name": "Vascularized Lymph Node Transfer", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "The National Institute of Lymphology", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 1000, "start_date": "2010-07", "completion_date": "2016-01", "has_results": false, "last_update_posted_date": "2014-06-06", "last_synced_at": "2026-10-23T15:21:27.338Z", "location_count": 3, "location_summary": "Chicago, Illinois • New Orleans, Louisiana • Charleston, South Carolina", "locations": [ { "city": "Chicago", "state": "Illinois" }, { "city": "New Orleans", "state": "Louisiana" }, { "city": "Charleston", "state": "South Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT01273909" }, { "nct_id": "NCT03834532", "title": "Living Well After Breast Surgery", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Breast Cancer Female", "Stage I Breast Cancer", "Stage II Breast Cancer", "Stage III Breast Cancer", "Ductal Carcinoma in Situ", "Ductal Breast Carcinoma", "Lobular Breast Carcinoma" ], "interventions": [ { "name": "Breast reconstruction decision aid", "type": "OTHER" }, { "name": "Educational website", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Texas at Austin", "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": 17, "start_date": "2019-02-18", "completion_date": "2021-06-11", "has_results": false, "last_update_posted_date": "2021-11-02", "last_synced_at": "2026-10-23T15:21:27.338Z", "location_count": 1, "location_summary": "Austin, Texas", "locations": [ { "city": "Austin", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT03834532" }, { "nct_id": "NCT01256528", "title": "Delayed-Delayed Breast Reconstruction", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Breast Cancer" ], "interventions": [ { "name": "Delayed Breast Reconstruction", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "M.D. Anderson Cancer Center", "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": 40, "start_date": "2010-12", "completion_date": "2015-09", "has_results": false, "last_update_posted_date": "2016-07-15", "last_synced_at": "2026-10-23T15:21:27.338Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT01256528" }, { "nct_id": "NCT06858293", "title": "Mental Imagery to Improve Quadriceps Strength Post Anterior Cruciate Ligament Reconstruction: a Feasibility Study", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Anterior Cruciate Ligament Reconstruction" ], "interventions": [ { "name": "Mental Imagery Open Chain", "type": "BEHAVIORAL" }, { "name": "Mental Imagery Closed Chain", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Marquette University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 20, "start_date": "2025-02-14", "completion_date": "2026-01-28", "has_results": false, "last_update_posted_date": "2025-03-10", "last_synced_at": "2026-10-23T15:21:27.338Z", "location_count": 1, "location_summary": "Milwaukee, Wisconsin", "locations": [ { "city": "Milwaukee", "state": "Wisconsin" } ], "official_url": "https://clinicaltrials.gov/study/NCT06858293" } ] }