{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=PCMS&page=2", "query": { "intervention": "PCMS", "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=PCMS&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-09-10T19:24:13.678Z", "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": "NCT03127826", "title": "Validation of the STarT Back Screening Tool in the Military", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Low Back Pain", "Lumbago", "Radiculopathy", "Intervertebral Disc Disorder" ], "interventions": [ { "name": "Risk Stratified Care", "type": "PROCEDURE" }, { "name": "Usual Care", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Brooke Army Medical Center", "sponsor_class": "FED", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "50 Years", "sex": "ALL", "summary": "18 Years to 50 Years" }, "enrollment_count": 290, "start_date": "2017-04-07", "completion_date": "2021-07-01", "has_results": true, "last_update_posted_date": "2026-06-24", "last_synced_at": "2026-09-10T19:24:13.678Z", "location_count": 1, "location_summary": "San Antonio, Texas", "locations": [ { "city": "San Antonio", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT03127826" }, { "nct_id": "NCT04956341", "title": "Auricular Acupuncture for Sleep Disturbances", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Sleep Disturbance" ], "interventions": [ { "name": "Auricular acupuncture", "type": "DEVICE" }, { "name": "Standard treatment", "type": "OTHER" } ], "intervention_types": [ "DEVICE", "OTHER" ], "sponsor": "Paul Crawford", "sponsor_class": "FED", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 180, "start_date": "2022-05-01", "completion_date": "2026-12", "has_results": false, "last_update_posted_date": "2026-01-12", "last_synced_at": "2026-09-10T19:24:13.678Z", "location_count": 1, "location_summary": "Nellis Air Force Base, Nevada", "locations": [ { "city": "Nellis Air Force Base", "state": "Nevada" } ], "official_url": "https://clinicaltrials.gov/study/NCT04956341" }, { "nct_id": "NCT06063603", "title": "Evaluation of a Pain Management Intervention Preparatory to a Future Pragmatic Trial, ASCENT Study", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Chronic Leukemia", "Hematopoietic and Lymphoid System Neoplasm", "Lymphoma", "Malignant Solid Neoplasm", "Multiple Myeloma" ], "interventions": [ { "name": "Acupuncture Therapy", "type": "PROCEDURE" }, { "name": "Cancer Pain Management", "type": "BEHAVIORAL" }, { "name": "Cognitive Behavior Therapy", "type": "BEHAVIORAL" }, { "name": "Discussion", "type": "PROCEDURE" }, { "name": "Educational Intervention", "type": "OTHER" }, { "name": "Exercise", "type": "OTHER" }, { "name": "Interview", "type": "OTHER" }, { "name": "Massage Therapy", "type": "PROCEDURE" }, { "name": "Mindfulness Relaxation", "type": "BEHAVIORAL" }, { "name": "Pain Therapy", "type": "PROCEDURE" }, { "name": "Palliative Therapy", "type": "OTHER" }, { "name": "Patient Navigation", "type": "BEHAVIORAL" }, { "name": "Referral", "type": "OTHER" }, { "name": "Spiritual Therapy", "type": "PROCEDURE" }, { "name": "Spiritual Care Referral", "type": "PROCEDURE" }, { "name": "Survey Administration", "type": "OTHER" } ], "intervention_types": [ "PROCEDURE", "BEHAVIORAL", "OTHER" ], "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": 51, "start_date": "2023-05-22", "completion_date": "2024-05-02", "has_results": true, "last_update_posted_date": "2025-09-18", "last_synced_at": "2026-09-10T19:24:13.678Z", "location_count": 2, "location_summary": "Scottsdale, Arizona • Rochester, Minnesota", "locations": [ { "city": "Scottsdale", "state": "Arizona" }, { "city": "Rochester", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT06063603" }, { "nct_id": "NCT02932748", "title": "Weight Management in Rural Communities", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Weight Loss", "Obesity", "Body Weight" ], "interventions": [ { "name": "Portion Controlled Meals (PCM)", "type": "DIETARY_SUPPLEMENT" }, { "name": "Group Phone (GP)", "type": "BEHAVIORAL" }, { "name": "Conventional Diet", "type": "DIETARY_SUPPLEMENT" }, { "name": "Individual Phone (IP)", "type": "BEHAVIORAL" }, { "name": "Enhanced Usual Care (EUC)", "type": "BEHAVIORAL" } ], "intervention_types": [ "DIETARY_SUPPLEMENT", "BEHAVIORAL" ], "sponsor": "University of Kansas", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": null, "sex": "ALL", "summary": "21 Years and older" }, "enrollment_count": 187, "start_date": "2017-01", "completion_date": "2021-10", "has_results": true, "last_update_posted_date": "2024-03-08", "last_synced_at": "2026-09-10T19:24:13.678Z", "location_count": 1, "location_summary": "Lawrence, Kansas", "locations": [ { "city": "Lawrence", "state": "Kansas" } ], "official_url": "https://clinicaltrials.gov/study/NCT02932748" }, { "nct_id": "NCT01679535", "title": "A Nutrition/Hygiene Education Program for the Prevention of Child Malnutrition in Rural Kenya", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Child Nutrition Disorders" ], "interventions": [ { "name": "nutrition and hygiene education", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of New Mexico", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "1 Month", "maximum_age": "6 Months", "sex": "ALL", "summary": "1 Month to 6 Months" }, "enrollment_count": 246, "start_date": "2011-11", "completion_date": "2014-12", "has_results": false, "last_update_posted_date": "2024-03-12", "last_synced_at": "2026-09-10T19:24:13.678Z", "location_count": 1, "location_summary": "Albuquerque, New Mexico", "locations": [ { "city": "Albuquerque", "state": "New Mexico" } ], "official_url": "https://clinicaltrials.gov/study/NCT01679535" }, { "nct_id": "NCT03591107", "title": "Trauma-informed Collaborative Care for Low-income African Americans With PTSD", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "PTSD" ], "interventions": [ { "name": "PTSD Care Management (PCM)", "type": "OTHER" }, { "name": "Minimally Enhanced Usual Care (MEU)", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "RAND", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 42, "start_date": "2018-10-12", "completion_date": "2020-03-30", "has_results": true, "last_update_posted_date": "2022-12-02", "last_synced_at": "2026-09-10T19:24:13.678Z", "location_count": 1, "location_summary": "New Orleans, Louisiana", "locations": [ { "city": "New Orleans", "state": "Louisiana" } ], "official_url": "https://clinicaltrials.gov/study/NCT03591107" }, { "nct_id": "NCT00578812", "title": "PCM Cervical Disc System", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Radiculopathy", "Myelopathy" ], "interventions": [ { "name": "Anterior Cervical Discectomy and Fusion (ACDF)", "type": "DEVICE" }, { "name": "PCM Cervical Disc", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "NuVasive", "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": 494, "start_date": "2005-01", "completion_date": "2014-08", "has_results": true, "last_update_posted_date": "2015-07-07", "last_synced_at": "2026-09-10T19:24:13.678Z", "location_count": 23, "location_summary": "Beverly Hills, California • Greenwood Village, Colorado • Washington D.C., District of Columbia + 18 more", "locations": [ { "city": "Beverly Hills", "state": "California" }, { "city": "Beverly Hills", "state": "California" }, { "city": "Greenwood Village", "state": "Colorado" }, { "city": "Washington D.C.", "state": "District of Columbia" }, { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT00578812" }, { "nct_id": "NCT05549661", "title": "Onvansertib for the Treatment of Recurrent or Refractory Chronic Myelomonocytic Leukemia and Myelodysplastic Syndrome/MPN Overlap Neoplasms", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Recurrent Chronic Myelomonocytic Leukemia", "Refractory Chronic Myelomonocytic Leukemia", "Myelodysplastic/Myeloproliferative Neoplasm, Not Otherwise Specified", "Recurrent Atypical Chronic Myeloid Leukemia", "Recurrent Myelodysplastic/Myeloproliferative Neoplasm", "Refractory Myelodysplastic/Myeloproliferative Neoplasm" ], "interventions": [ { "name": "Biospecimen Collection", "type": "PROCEDURE" }, { "name": "Bone Marrow Aspiration and Biopsy", "type": "PROCEDURE" }, { "name": "Onvansertib", "type": "DRUG" }, { "name": "Ultrasound Imaging", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE", "DRUG" ], "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": 25, "start_date": "2023-04-04", "completion_date": "2027-12-01", "has_results": false, "last_update_posted_date": "2026-06-22", "last_synced_at": "2026-09-10T19:24:13.678Z", "location_count": 1, "location_summary": "Rochester, Minnesota", "locations": [ { "city": "Rochester", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT05549661" }, { "nct_id": "NCT02273206", "title": "Collaborative Care to Reduce Depression and Increase Cancer Screening Among Low-Income Urban Women", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Depression", "Breast Cancer Screening", "Cervical Cancer Screening", "Colorectal Cancer Screening" ], "interventions": [ { "name": "Prevention Care Management for Depression and Cancer Screening", "type": "BEHAVIORAL" }, { "name": "Prevention Care Management for Cancer Screening", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Clinical Directors Network", "sponsor_class": "NETWORK", "healthy_volunteers": false, "eligibility": { "minimum_age": "50 Years", "maximum_age": "64 Years", "sex": "FEMALE", "summary": "50 Years to 64 Years · Female only" }, "enrollment_count": 802, "start_date": "2014-01", "completion_date": "2017-12-31", "has_results": true, "last_update_posted_date": "2020-03-12", "last_synced_at": "2026-09-10T19:24:13.678Z", "location_count": 8, "location_summary": "The Bronx, New York", "locations": [ { "city": "The Bronx", "state": "New York" }, { "city": "The Bronx", "state": "New York" }, { "city": "The Bronx", "state": "New York" }, { "city": "The Bronx", "state": "New York" }, { "city": "The Bronx", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT02273206" }, { "nct_id": "NCT01873976", "title": "Cardiac Biomarkers in Pediatric Cardiomyopathy (PCM Biomarkers)", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Dilated Cardiomyopathy", "Hypertrophic Cardiomyopathy" ], "interventions": [], "intervention_types": [], "sponsor": "Wayne State University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": "20 Years", "sex": "ALL", "summary": "Up to 20 Years" }, "enrollment_count": 288, "start_date": "2013-06", "completion_date": "2019-06", "has_results": false, "last_update_posted_date": "2026-08-19", "last_synced_at": "2026-09-10T19:24:13.678Z", "location_count": 12, "location_summary": "Aurora, Colorado • Chicago, Illinois • Boston, Massachusetts + 9 more", "locations": [ { "city": "Aurora", "state": "Colorado" }, { "city": "Chicago", "state": "Illinois" }, { "city": "Boston", "state": "Massachusetts" }, { "city": "St Louis", "state": "Missouri" }, { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT01873976" } ] }