{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Medical+Data+Collection", "query": { "intervention": "Medical Data Collection" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 642, "total_pages": 65, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Medical+Data+Collection&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-09-08T18:00:52.631Z", "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": "NCT05671861", "title": "Evaluating a Low-Cost Therapeutic Device in Managing Head and Neck Cancer Patients With Radiation-Related Trismus", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Trismus", "Head and Neck Cancer" ], "interventions": [ { "name": "Trismus Device Prototype", "type": "DEVICE" }, { "name": "Questionnaires", "type": "OTHER" }, { "name": "Mobile Application", "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": 35, "start_date": "2023-04-27", "completion_date": "2028-03-31", "has_results": false, "last_update_posted_date": "2026-01-13", "last_synced_at": "2026-09-08T18:00:52.631Z", "location_count": 1, "location_summary": "San Francisco, California", "locations": [ { "city": "San Francisco", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT05671861" }, { "nct_id": "NCT05394324", "title": "A Post-market Clinical Study to Collect Safety and Performance Data on Johnson & Johnson Surgical Vision Products", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Refractive Error", "Glaucoma", "Cataracts", "Clear Lens Exchange" ], "interventions": [ { "name": "Intervention", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Johnson & Johnson Surgical Vision, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 1674, "start_date": "2022-06-21", "completion_date": "2025-05-31", "has_results": false, "last_update_posted_date": "2025-07-20", "last_synced_at": "2026-09-08T18:00:52.631Z", "location_count": 4, "location_summary": "Dothan, Alabama • Bakersfield, California • Bloomington, Minnesota + 1 more", "locations": [ { "city": "Dothan", "state": "Alabama" }, { "city": "Bakersfield", "state": "California" }, { "city": "Bloomington", "state": "Minnesota" }, { "city": "McAllen", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT05394324" }, { "nct_id": "NCT05268991", "title": "Aging and Frailty Study", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Effects of Chemotherapy", "Aging", "Frailty" ], "interventions": [ { "name": "Geriatric Assessments and Frailty Indices", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Wake Forest University Health Sciences", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "65 Years", "maximum_age": null, "sex": "ALL", "summary": "65 Years and older" }, "enrollment_count": 25, "start_date": "2022-05-02", "completion_date": "2025-06-13", "has_results": false, "last_update_posted_date": "2025-08-01", "last_synced_at": "2026-09-08T18:00:52.631Z", "location_count": 1, "location_summary": "Winston-Salem, North Carolina", "locations": [ { "city": "Winston-Salem", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT05268991" }, { "nct_id": "NCT00101868", "title": "Value of Technology to Transfer Discharge Information", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Information Dissemination", "Interprofessional Relations" ], "interventions": [ { "name": "Discharge communication software", "type": "DEVICE" }, { "name": "Usual care discharge process", "type": "OTHER" } ], "intervention_types": [ "DEVICE", "OTHER" ], "sponsor": "Agency for Healthcare Research and Quality (AHRQ)", "sponsor_class": "FED", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 631, "start_date": "2004-12", "completion_date": "2007-08", "has_results": true, "last_update_posted_date": "2012-05-15", "last_synced_at": "2026-09-08T18:00:52.631Z", "location_count": 1, "location_summary": "Peoria, Illinois", "locations": [ { "city": "Peoria", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT00101868" }, { "nct_id": "NCT02529618", "title": "Field Implementation of iDETECT", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Concussion", "Brain Trauma" ], "interventions": [ { "name": "integrated Display Enhanced Testing for Cognitive Impairment and mild traumatic brain injury (iDETECT)", "type": "DEVICE" }, { "name": "Riddell High Impact Technology (HIT) System", "type": "DEVICE" }, { "name": "i1 Biometrics Vector Mouth Guard", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Emory University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "14 Years", "maximum_age": null, "sex": "ALL", "summary": "14 Years and older" }, "enrollment_count": 124, "start_date": "2015-08", "completion_date": "2016-02", "has_results": false, "last_update_posted_date": "2016-03-04", "last_synced_at": "2026-09-08T18:00:52.631Z", "location_count": 4, "location_summary": "Atlanta, Georgia • College Park, Georgia • Marietta, Georgia + 1 more", "locations": [ { "city": "Atlanta", "state": "Georgia" }, { "city": "College Park", "state": "Georgia" }, { "city": "Marietta", "state": "Georgia" }, { "city": "Roswell", "state": "Georgia" } ], "official_url": "https://clinicaltrials.gov/study/NCT02529618" }, { "nct_id": "NCT06451341", "title": "IMplementation of CAB+RPV LA for People With HIV in Non-Metropolitan Areas", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "HIV" ], "interventions": [ { "name": "Acceptability of Intervention Measure (AIM)", "type": "BEHAVIORAL" }, { "name": "Intervention Appropriateness Measure (IAM)", "type": "BEHAVIORAL" }, { "name": "Feasibility of Intervention Measure (FIM)", "type": "BEHAVIORAL" }, { "name": "HIV Stigma Scale Questionnaire", "type": "BEHAVIORAL" }, { "name": "HIV Treatment Satisfaction Questionnaire status version (HIVTSQs12)", "type": "BEHAVIORAL" }, { "name": "HIV Treatment Satisfaction Questionnaire change version (HIVTSQc12)", "type": "BEHAVIORAL" }, { "name": "Needs and Barriers Assessment", "type": "BEHAVIORAL" }, { "name": "Pre-visit Outreach", "type": "BEHAVIORAL" }, { "name": "Qualitative interview - patient participants", "type": "BEHAVIORAL" }, { "name": "Staff education", "type": "BEHAVIORAL" }, { "name": "Staff Month 7 and 15 Survey - Staff Burden and Engagement", "type": "BEHAVIORAL" }, { "name": "Qualitative interview - staff", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Nebraska", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "19 Years", "maximum_age": null, "sex": "ALL", "summary": "19 Years and older" }, "enrollment_count": 75, "start_date": "2024-07-01", "completion_date": "2028-05", "has_results": false, "last_update_posted_date": "2026-07-24", "last_synced_at": "2026-09-08T18:00:52.631Z", "location_count": 4, "location_summary": "Harlan, Iowa • Shenandoah, Iowa • Grand Island, Nebraska + 1 more", "locations": [ { "city": "Harlan", "state": "Iowa" }, { "city": "Shenandoah", "state": "Iowa" }, { "city": "Grand Island", "state": "Nebraska" }, { "city": "Omaha", "state": "Nebraska" } ], "official_url": "https://clinicaltrials.gov/study/NCT06451341" }, { "nct_id": "NCT05349422", "title": "Addressing Antihypertensive Medication Adherence Through EHR-enabled Teamlets in Primary Care", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Blood Pressure", "Medication Adherence" ], "interventions": [ { "name": "Electronic Health Record (EHR) Enabled Teamlets", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "NYU Langone Health", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 1842, "start_date": "2022-10-06", "completion_date": "2025-05-11", "has_results": true, "last_update_posted_date": "2026-06-30", "last_synced_at": "2026-09-08T18:00:52.631Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT05349422" }, { "nct_id": "NCT03758521", "title": "Natural History Study of Patients With Succinic Semialdehyde Dehydrogenase (SSADH) Deficiency", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Succinic Semialdehyde Dehydrogenase Deficiency" ], "interventions": [ { "name": "Transcranial magnetic stimulation (TMS)", "type": "DEVICE" }, { "name": "Magnetic resonance imaging (MRI)", "type": "DEVICE" }, { "name": "Electroencephalogram (EEG)", "type": "DEVICE" }, { "name": "Bio-specimen Collection", "type": "PROCEDURE" } ], "intervention_types": [ "DEVICE", "PROCEDURE" ], "sponsor": "Boston Children's Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 55, "start_date": "2019-01-15", "completion_date": "2029-06", "has_results": false, "last_update_posted_date": "2026-01-13", "last_synced_at": "2026-09-08T18:00:52.631Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT03758521" }, { "nct_id": "NCT00256386", "title": "LabAlert: Enhancing Medication Safety Through Electronic Interventions to Improve Laboratory Monitoring", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Safety" ], "interventions": [ { "name": "Electronic Medical Record (EMR) to clinician's in-basket", "type": "DEVICE" }, { "name": "Automated Voice Message (AVM) reminder to patient's phone", "type": "DEVICE" }, { "name": "Pharmacy Team phone call-letter followup", "type": "PROCEDURE" } ], "intervention_types": [ "DEVICE", "PROCEDURE" ], "sponsor": "Kaiser Permanente", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 800, "start_date": "2004-01", "completion_date": "2005-03", "has_results": false, "last_update_posted_date": "2006-11-30", "last_synced_at": "2026-09-08T18:00:52.631Z", "location_count": 1, "location_summary": "Portland, Oregon", "locations": [ { "city": "Portland", "state": "Oregon" } ], "official_url": "https://clinicaltrials.gov/study/NCT00256386" }, { "nct_id": "NCT01403402", "title": "Congenital Muscle Disease Study of Patient and Family Reported Medical Information", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Congenital Muscular Dystrophy With ITGA7 (Integrin Alpha-7) Deficiency", "Alpha-Dystroglycanopathy (Congenital Muscular Dystrophy and Abnormal Glycosylation of Dystroglycan With Severe Epilepsy)", "Alpha-Dystroglycanopathy (Congenital Muscular Dystrophy With Fatty Liver and Infantile-onset Cataract Caused by TRAPPC11 Mutations)", "Alpha-Dystroglycanopathy (Congenital Muscular Dystrophy With Hypoglycosylation of Dystroglycan)", "Alpha-Dystroglycanopathy (Congenital Muscular Dystrophy With Hypoglycosylation of Dystroglycan and Epilepsy)", "Alpha-Dystroglycanopathy (Dystroglycanopathy, Congenital With or Without Mental Retardation (Formerly MDC1C))", "Alpha-Dystroglycanopathy (Fukuyama CMD)", "Alpha-Dystroglycanopathy (LGMDR09 FKRP Related (Formerly LGMD2I))", "Alpha-Dystroglycanopathy (LGMDR11 POMT1 Related (Formerly LGMD2K))", "Alpha-Dystroglycanopathy (LGMDR13 FKTN Related (Formerly LGMD2M))", "Alpha-Dystroglycanopathy (LGMDR14 POMT2 Related (Formerly LGMD2N))", "Alpha-Dystroglycanopathy (LGMDR15 POMGnT1 Related (Formerly LGMD2O))", "Alpha-Dystroglycanopathy (LGMDR19 GMPPB Related (Formerly LGMD2T))", "Alpha-Dystroglycanopathy (LGMDR20 ISPD Related (Formerly LGMD2U))", "Alpha-Dystroglycanopathy (LGMDR24 POMGnT2 Related)", "Alpha-Dystroglycanopathy (Muscle Eye Brain Disease (MEB))", "Alpha-Dystroglycanopathy (Walker Warburg Syndrome (WWS))", "Choline Kinase B Receptor - CHKB", "Collagen VI Related Disorders", "Collagen XII Related Disorders", "Congenital Muscular Dystrophy Not Otherwise Specified (Including Merosin Positive)", "Congenital Muscular Dystrophy With Cataracts and Intellectual Disability (MDCCAID)", "Congenital Muscular Dystrophy With Joint Hyperlaxity", "Congenital Muscular Dystrophy With Rigid Spine Related to ACTA1", "Emery-Dreifuss Muscular Dystrophy", "GOLGA2-related Congenital Muscle Dystrophy With Brain Involvement", "LMNA Related Disorders", "Merosin Deficient CMD (Full or Partial)", "Nesprin Related MD (SYNE1)", "SELENON Related Disorders (Previously Known as SEPN1)", "SELENON Related Myopathy (Aka SEPN1)", "Telethonin CMD", "Congenital Myasthenic Syndrome", "Limb-Girdle Muscular Dystrophy", "LGMDD01 - DNAJB6 (Formerly LGMD1D)", "LGMDD05 - Collagen VI Related Bethlem Myopathy (Dominant)", "LGMDR07 - Telethonin (TCAP) Related (Formerly LGMD2G)", "LGMDR08 - TRIM Related (Formerly LGMD2H)", "LGMDR09 - FKRP Related (Formerly LGMD2I)", "LGMDR10 - Titin (TTN) Related (Formerly LGMD2J)", "LGMDR11 - POMT1 Related (Formerly LGMD2K)", "LGMDR13 - Fukutin (FKTN) Related (Formerly LGMD2M)", "LGMDR14 - POMT2 Related (Formerly LGMD2N)", "LGMDR15 - POMGnT1 Related (Formerly LGMD2O)", "LGMDR16 - DAG1 Related Dystroglycanopathy (Formerly LGMD2P)", "LGMDR17 - Plectin (PLEC) Related (Formerly LGMD2Q)", "LGMDR18 - TRAPPC11 Related (Formerly LGMD2S)", "LGMDR19 - GMPPB Related (Formerly LGMD2T)", "LGMDR20 - ISPD Related (Formerly LGMD2U)", "LGMDR22 - Collagen VI Related Bethlem Myopathy (Recessive)", "LGMDR23 - LAMA2 Related", "LGMDR24 - POMGnT2 Related" ], "interventions": [], "intervention_types": [], "sponsor": "Cure CMD", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 4000, "start_date": "2009-09", "completion_date": "2029-09", "has_results": false, "last_update_posted_date": "2021-08-09", "last_synced_at": "2026-09-08T18:00:52.631Z", "location_count": 1, "location_summary": "Lakewood, California", "locations": [ { "city": "Lakewood", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT01403402" } ] }