{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=High+pro&page=2", "query": { "intervention": "High pro", "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=High+pro&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-09-09T18:27:17.331Z", "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": "NCT05492500", "title": "A Study of Ponsegromab in People With Heart Failure", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Heart Failure" ], "interventions": [ { "name": "Main cohort (Cohort A): Ponsegromab low dose", "type": "DRUG" }, { "name": "Main cohort (Cohort A): Ponsegromab medium dose", "type": "DRUG" }, { "name": "Main cohort (Cohort A): ponsegromab high dose", "type": "DRUG" }, { "name": "Main cohort (Cohort A): Matched placebo", "type": "OTHER" }, { "name": "Open-label, PK Cohort (Cohort B): ponsegromab low dose", "type": "DRUG" }, { "name": "Open-label, PK Cohort (Cohort B): ponsegromab medium dose", "type": "DRUG" }, { "name": "Open-label, PK Cohort (Cohort B): ponsegromab high dose", "type": "DRUG" }, { "name": "Optional Cohort C: Ponsegromab low dose", "type": "DRUG" }, { "name": "Optional Cohort C: Matched placebo", "type": "OTHER" }, { "name": "Optional Cohort D: Ponsegromab high dose", "type": "DRUG" }, { "name": "Optional Cohort D: Matched placebo", "type": "OTHER" } ], "intervention_types": [ "DRUG", "OTHER" ], "sponsor": "Pfizer", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 455, "start_date": "2022-09-26", "completion_date": "2025-03-05", "has_results": true, "last_update_posted_date": "2026-03-18", "last_synced_at": "2026-09-09T18:27:17.331Z", "location_count": 22, "location_summary": "Fairhope, Alabama • Los Angeles, California • Washington D.C., District of Columbia + 13 more", "locations": [ { "city": "Fairhope", "state": "Alabama" }, { "city": "Los Angeles", "state": "California" }, { "city": "Washington D.C.", "state": "District of Columbia" }, { "city": "Atlanta", "state": "Georgia" }, { "city": "Hazel Crest", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT05492500" }, { "nct_id": "NCT04796571", "title": "Care Coordination and Proactive Care to Improve Utilization of Resources and Reduce Expenditure in High Risk Inflammatory Bowel Disease (IBD) Patients", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Inflammatory Bowel Diseases" ], "interventions": [ { "name": "Proactive Symptom Monitoring and Care Coordination", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Michigan", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "90 Years", "sex": "ALL", "summary": "18 Years to 90 Years" }, "enrollment_count": 425, "start_date": "2019-01-01", "completion_date": "2020-03-01", "has_results": false, "last_update_posted_date": "2021-03-15", "last_synced_at": "2026-09-09T18:27:17.331Z", "location_count": 1, "location_summary": "Ann Arbor, Michigan", "locations": [ { "city": "Ann Arbor", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT04796571" }, { "nct_id": "NCT07020273", "title": "CONNECT Cancer Survivors With Tobacco Treatment", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Tobacco Use", "Tobacco Use Cessation", "Smoking Cessation", "Nicotine Addiction", "Tobacco Smoking" ], "interventions": [ { "name": "ELEVATE", "type": "BEHAVIORAL" }, { "name": "ELEVATE-S", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Washington University School of Medicine", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 3543, "start_date": "2025-07-01", "completion_date": "2026-09-30", "has_results": false, "last_update_posted_date": "2026-07-10", "last_synced_at": "2026-09-09T18:27:17.331Z", "location_count": 1, "location_summary": "St Louis, Missouri", "locations": [ { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT07020273" }, { "nct_id": "NCT04845685", "title": "A Study to Evaluate Continuous Glucose Monitor in Hospitalized, Post-operative Patients With Diabetes Mellitus", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Diabetes Mellitus" ], "interventions": [ { "name": "Continuous Glucose Monitor (CGM)", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Mayo Clinic", "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": "2026-06", "completion_date": "2026-12-08", "has_results": false, "last_update_posted_date": "2026-07-16", "last_synced_at": "2026-09-09T18:27:17.331Z", "location_count": 1, "location_summary": "Jacksonville, Florida", "locations": [ { "city": "Jacksonville", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT04845685" }, { "nct_id": "NCT06270043", "title": "Focal Therapy for Localized Prostate Cancer", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Prostate Cancer" ], "interventions": [ { "name": "Focal Therapy", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "University of California, San Diego", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "MALE", "summary": "18 Years and older · Male only" }, "enrollment_count": 500, "start_date": "2024-02-01", "completion_date": "2034-02-01", "has_results": false, "last_update_posted_date": "2024-02-26", "last_synced_at": "2026-09-09T18:27:17.331Z", "location_count": 1, "location_summary": "La Jolla, California", "locations": [ { "city": "La Jolla", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT06270043" }, { "nct_id": "NCT00223717", "title": "Treatment of Supine Hypertension in Autonomic Failure", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Hypertension" ], "interventions": [ { "name": "Clonidine", "type": "DRUG" }, { "name": "Nitroglycerin transdermal", "type": "DRUG" }, { "name": "Dipyridamole/ Aspirin (Aggrenox)", "type": "DRUG" }, { "name": "Desmopressin (DDAVP)", "type": "DRUG" }, { "name": "Sildenafil", "type": "DRUG" }, { "name": "Nifedipine", "type": "DRUG" }, { "name": "Hydralazine", "type": "DRUG" }, { "name": "Hydrochlorothiazide", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" }, { "name": "Bosentan", "type": "DRUG" }, { "name": "Diltiazem", "type": "DRUG" }, { "name": "Eplerenone", "type": "DRUG" }, { "name": "guanfacine", "type": "DRUG" }, { "name": "L-arginine", "type": "DIETARY_SUPPLEMENT" }, { "name": "captopril", "type": "DRUG" }, { "name": "carbidopa", "type": "DRUG" }, { "name": "losartan", "type": "DRUG" }, { "name": "metoprolol tartrate", "type": "DRUG" }, { "name": "nebivolol hydrochloride", "type": "DRUG" }, { "name": "prazosin hydrochloride", "type": "DRUG" }, { "name": "tamsulosin hydrochloride", "type": "DRUG" }, { "name": "Head-up tilt.", "type": "OTHER" }, { "name": "aliskiren", "type": "DRUG" }, { "name": "Local heat stress", "type": "OTHER" } ], "intervention_types": [ "DRUG", "DIETARY_SUPPLEMENT", "OTHER" ], "sponsor": "Vanderbilt University", "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": 152, "start_date": "2001-01", "completion_date": "2017-01", "has_results": false, "last_update_posted_date": "2017-10-13", "last_synced_at": "2026-09-09T18:27:17.331Z", "location_count": 1, "location_summary": "Nashville, Tennessee", "locations": [ { "city": "Nashville", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT00223717" }, { "nct_id": "NCT07380243", "title": "Pathways to Prevention Food-is-Medicine Trial", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Heart Disease", "Cardiovascular Health Status" ], "interventions": [ { "name": "Nutrition Education", "type": "BEHAVIORAL" }, { "name": "PRO-CVH", "type": "BEHAVIORAL" }, { "name": "Healthy Conversation Skills", "type": "BEHAVIORAL" }, { "name": "Medically tailored groceries/cooking classes", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Amrik Singh Khalsa", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "6 Years", "maximum_age": null, "sex": "ALL", "summary": "6 Years and older" }, "enrollment_count": 120, "start_date": "2026-02-26", "completion_date": "2026-12-01", "has_results": false, "last_update_posted_date": "2026-05-15", "last_synced_at": "2026-09-09T18:27:17.331Z", "location_count": 1, "location_summary": "Columbus, Ohio", "locations": [ { "city": "Columbus", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT07380243" }, { "nct_id": "NCT07452406", "title": "Protocolized Weaning of High-Flow Nasal Cannula in Adult Patients", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Acute Hypoxemic Respiratory Failure", "High-Flow Nasal Cannula Therapy" ], "interventions": [ { "name": "Protocolized HFNC Weaning Strategy", "type": "BEHAVIORAL" }, { "name": "Usual Care HFNC Weaning", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Rush University Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 2000, "start_date": "2026-09-01", "completion_date": "2028-06-28", "has_results": false, "last_update_posted_date": "2026-06-10", "last_synced_at": "2026-09-09T18:27:17.331Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT07452406" }, { "nct_id": "NCT05509270", "title": "Efficacy of Communication Modalities for Promoting Flu Shots", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Influenza Vaccination", "Health Promotion", "Health Behavior", "Risk Reduction" ], "interventions": [ { "name": "Letter", "type": "BEHAVIORAL" }, { "name": "Patient portal", "type": "BEHAVIORAL" }, { "name": "SMS", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Geisinger Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 43225, "start_date": "2022-09-06", "completion_date": "2022-10-04", "has_results": false, "last_update_posted_date": "2022-10-12", "last_synced_at": "2026-09-09T18:27:17.331Z", "location_count": 1, "location_summary": "Danville, Pennsylvania", "locations": [ { "city": "Danville", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT05509270" }, { "nct_id": "NCT04130867", "title": "Rehabilitation Manometry Study", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Oropharyngeal Dysphagia" ], "interventions": [ { "name": "pHRM", "type": "PROCEDURE" }, { "name": "VFSS", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "University of Wisconsin, Madison", "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": 4, "start_date": "2020-11-11", "completion_date": "2021-04-21", "has_results": false, "last_update_posted_date": "2025-10-29", "last_synced_at": "2026-09-09T18:27:17.331Z", "location_count": 1, "location_summary": "Madison, Wisconsin", "locations": [ { "city": "Madison", "state": "Wisconsin" } ], "official_url": "https://clinicaltrials.gov/study/NCT04130867" } ] }