{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?page=6&sponsor=Ohio+University", "query": { "sponsor": "Ohio University", "page": 6 }, "page_size": 10 }, "pagination": { "page": 6, "page_size": 10, "total_count": 1626, "total_pages": 163, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?page=7&sponsor=Ohio+University&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?page=5&sponsor=Ohio+University&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-12T01:04:19.089Z", "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": "NCT05102383", "title": "Evaluation of Wear Experience With a Water Surface Daily Disposable Contact Lens", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Contact Lens" ], "interventions": [ { "name": "Comfilcon A Toric contact lenses", "type": "DEVICE" }, { "name": "Verofilcon A for Astigmatism Daily Disposable contact lenses", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Ohio State University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "40 Years", "sex": "ALL", "summary": "18 Years to 40 Years" }, "enrollment_count": 34, "start_date": "2021-11-15", "completion_date": "2022-04-19", "has_results": true, "last_update_posted_date": "2025-11-25", "last_synced_at": "2026-10-12T01:04:19.089Z", "location_count": 1, "location_summary": "Columbus, Ohio", "locations": [ { "city": "Columbus", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT05102383" }, { "nct_id": "NCT06523946", "title": "Pacific Islander Physical Activity Project", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Physical Inactivity" ], "interventions": [ { "name": "Diabetes Prevention Program (DPP) (shortened)", "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": 150, "start_date": "2025-05-19", "completion_date": "2028-06-30", "has_results": false, "last_update_posted_date": "2026-08-03", "last_synced_at": "2026-10-12T01:04:19.089Z", "location_count": 1, "location_summary": "Salt Lake City, Utah", "locations": [ { "city": "Salt Lake City", "state": "Utah" } ], "official_url": "https://clinicaltrials.gov/study/NCT06523946" }, { "nct_id": "NCT05289869", "title": "A Pilot Study: High Versus Low Oxytocin Dosing for Induction of Labor in Pregnant Patients With Obesity", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Pregnant Patients With Obesity" ], "interventions": [ { "name": "High-dose oxytocin", "type": "DRUG" }, { "name": "Low-dose oxytocin", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Ohio State University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "50 Years", "sex": "FEMALE", "summary": "18 Years to 50 Years · Female only" }, "enrollment_count": 20, "start_date": "2022-04-06", "completion_date": "2022-10-28", "has_results": true, "last_update_posted_date": "2023-11-29", "last_synced_at": "2026-10-12T01:04:19.089Z", "location_count": 1, "location_summary": "Columbus, Ohio", "locations": [ { "city": "Columbus", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT05289869" }, { "nct_id": "NCT01569854", "title": "Genetic Influence on Statin Pharmacodynamics", "overall_status": "WITHDRAWN", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Hyperlipidemia", "Hypercholesterolemia", "Dyslipidemia" ], "interventions": [], "intervention_types": [], "sponsor": "Ohio State University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 0, "start_date": "2012-03", "completion_date": "2022-03", "has_results": false, "last_update_posted_date": "2016-09-27", "last_synced_at": "2026-10-12T01:04:19.089Z", "location_count": 1, "location_summary": "Columbus, Ohio", "locations": [ { "city": "Columbus", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT01569854" }, { "nct_id": "NCT02087072", "title": "Collaborative Home Visits to Reduce Hospital Readmissions and Improve Medication Use During Transitions of Care", "overall_status": "WITHDRAWN", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Transitional Care Coordination", "Home Visits" ], "interventions": [ { "name": "Collaborative visit with provider and pharmacist", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Ohio State University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 0, "start_date": "2013-10", "completion_date": "2014-12", "has_results": false, "last_update_posted_date": "2022-09-30", "last_synced_at": "2026-10-12T01:04:19.089Z", "location_count": 1, "location_summary": "Columbus, Ohio", "locations": [ { "city": "Columbus", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT02087072" }, { "nct_id": "NCT04164069", "title": "Dasatinib for the Prevention of Oxaliplatin-Induced Neuropathy in Patients With Metastatic Gastrointestinal Cancer Receiving FOLFOX Chemotherapy With or Without Bevacizumab", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Advanced Colorectal Carcinoma", "Metastatic Colorectal Carcinoma", "Stage IV Colorectal Cancer AJCC v8", "Stage IVA Colorectal Cancer AJCC v8", "Stage IVB Colorectal Cancer AJCC v8", "Stage IVC Colorectal Cancer AJCC v8", "Stage II Colon Cancer", "Stage II Rectal Cancer", "Stage III Colon Cancer", "Stage III Rectal Cancer", "Esophageal Cancer", "Pancreatic Cancer", "Bile Duct Cancer", "Gastric Cancer", "Gall Bladder Cancer", "Small Bowel Adenocarcinoma" ], "interventions": [ { "name": "Bevacizumab", "type": "BIOLOGICAL" }, { "name": "Dasatinib", "type": "DRUG" }, { "name": "Fluorouracil", "type": "DRUG" }, { "name": "Leucovorin", "type": "DRUG" }, { "name": "Leucovorin Calcium", "type": "DRUG" }, { "name": "Oxaliplatin", "type": "DRUG" }, { "name": "Quality-of-Life Assessment", "type": "OTHER" } ], "intervention_types": [ "BIOLOGICAL", "DRUG", "OTHER" ], "sponsor": "Anne Noonan", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 9, "start_date": "2020-09-02", "completion_date": "2023-06-22", "has_results": false, "last_update_posted_date": "2024-12-27", "last_synced_at": "2026-10-12T01:04:19.089Z", "location_count": 1, "location_summary": "Columbus, Ohio", "locations": [ { "city": "Columbus", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT04164069" }, { "nct_id": "NCT03908112", "title": "Interventions for Convergence Insufficiency in Concussed Children", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Concussion", "Convergence Insufficiency" ], "interventions": [ { "name": "Standard Community Concussion Care (SC)", "type": "BEHAVIORAL" }, { "name": "SC plus Simple Convergence Exercises (SC+)", "type": "BEHAVIORAL" }, { "name": "SC plus Office-based Vergence/Accommodative Therapy (SC+OBVAT)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Mitchell Scheiman", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "11 Years", "maximum_age": "17 Years", "sex": "ALL", "summary": "11 Years to 17 Years" }, "enrollment_count": 264, "start_date": "2021-04-01", "completion_date": "2025-03-31", "has_results": false, "last_update_posted_date": "2020-10-23", "last_synced_at": "2026-10-12T01:04:19.089Z", "location_count": 8, "location_summary": "Birmingham, Alabama • Fullerton, California • Palo Alto, California + 5 more", "locations": [ { "city": "Birmingham", "state": "Alabama" }, { "city": "Fullerton", "state": "California" }, { "city": "Palo Alto", "state": "California" }, { "city": "Boston", "state": "Massachusetts" }, { "city": "Newark", "state": "New Jersey" } ], "official_url": "https://clinicaltrials.gov/study/NCT03908112" }, { "nct_id": "NCT02524366", "title": "A Study of Transcorporal Versus Standard Artificial Urinary Sphincter Placement", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Stress Urinary Incontinence" ], "interventions": [ { "name": "Artificial Urinary Sphincter", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of Minnesota", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "85 Years", "sex": "MALE", "summary": "18 Years to 85 Years · Male only" }, "enrollment_count": 0, "start_date": "2015-09", "completion_date": "2017-11", "has_results": false, "last_update_posted_date": "2019-07-22", "last_synced_at": "2026-10-12T01:04:19.089Z", "location_count": 1, "location_summary": "Minneapolis, Minnesota", "locations": [ { "city": "Minneapolis", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT02524366" }, { "nct_id": "NCT04007094", "title": "Single-Armed Use of ViviGen Cellular Bone Matrix in Patients Undergoing Posterolateral Lumbar Surgery", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Degenerative Disc Disease", "Spinal Stenosis", "Spondylosis", "Spondylolisthesis" ], "interventions": [ { "name": "ViviGen Cellular Bone Matrix", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Ohio State University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 21, "start_date": "2019-02-12", "completion_date": "2022-01-21", "has_results": true, "last_update_posted_date": "2024-01-24", "last_synced_at": "2026-10-12T01:04:19.089Z", "location_count": 1, "location_summary": "Columbus, Ohio", "locations": [ { "city": "Columbus", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT04007094" }, { "nct_id": "NCT03407612", "title": "Outcomes of CPM Usage Following Arthroscopic Acetabular Labral Repair", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Femoro Acetabular Impingement", "Pain, Postoperative", "Hip Labral Tear" ], "interventions": [ { "name": "Continuous Passive Motion", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Ohio State University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "14 Years", "maximum_age": "50 Years", "sex": "ALL", "summary": "14 Years to 50 Years" }, "enrollment_count": 54, "start_date": "2013-02-15", "completion_date": "2015-06-25", "has_results": true, "last_update_posted_date": "2020-10-08", "last_synced_at": "2026-10-12T01:04:19.089Z", "location_count": 1, "location_summary": "Columbus, Ohio", "locations": [ { "city": "Columbus", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT03407612" } ] }