{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Data+Collection+and+Analysis&page=5", "query": { "intervention": "Data Collection and Analysis", "page": 5 }, "page_size": 10 }, "pagination": { "page": 5, "page_size": 10, "total_count": 460, "total_pages": 46, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Data+Collection+and+Analysis&page=6&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Data+Collection+and+Analysis&page=4&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-23T23:35:35.614Z", "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": "NCT02307318", "title": "Heart and Hands Study II: A Retrospective Data Collection & Analysis Project", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1", "PHASE2" ], "conditions": [ "Thrombosis" ], "interventions": [ { "name": "SoftSeal Hemostatic Pad", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "HealthEast Care System", "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": "2014-11", "completion_date": "2015-06", "has_results": true, "last_update_posted_date": "2017-01-11", "last_synced_at": "2026-10-23T23:35:35.614Z", "location_count": 1, "location_summary": "Saint Paul, Minnesota", "locations": [ { "city": "Saint Paul", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT02307318" }, { "nct_id": "NCT02551718", "title": "High Throughput Drug Sensitivity Assay and Genomics- Guided Treatment of Patients With Relapsed or Refractory Acute Leukemia", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Recurrent Acute Leukemia of Ambiguous Lineage", "Recurrent Acute Lymphoblastic Leukemia", "Recurrent Acute Myeloid Leukemia", "Refractory Acute Lymphoblastic Leukemia", "Refractory Acute Myeloid Leukemia", "Refractory Acute Leukemia of Ambiguous Lineage" ], "interventions": [ { "name": "Chemosensitivity Assay", "type": "OTHER" }, { "name": "Cytology Specimen Collection Procedure", "type": "OTHER" }, { "name": "Gene Expression Analysis", "type": "GENETIC" }, { "name": "Genetic Variation Analysis", "type": "GENETIC" }, { "name": "In Vitro Sensitivity-Directed Chemotherapy", "type": "DRUG" } ], "intervention_types": [ "OTHER", "GENETIC", "DRUG" ], "sponsor": "University of Washington", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "3 Years", "maximum_age": null, "sex": "ALL", "summary": "3 Years and older" }, "enrollment_count": 34, "start_date": "2015-09-11", "completion_date": "2021-05-13", "has_results": true, "last_update_posted_date": "2022-06-30", "last_synced_at": "2026-10-23T23:35:35.614Z", "location_count": 1, "location_summary": "Seattle, Washington", "locations": [ { "city": "Seattle", "state": "Washington" } ], "official_url": "https://clinicaltrials.gov/study/NCT02551718" }, { "nct_id": "NCT04428723", "title": "Mechanisms of Hypoglycemia in Patients Without Diabetes", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Hypoglycemia" ], "interventions": [ { "name": "Entry of demographic and medical history data into a deidentified database", "type": "OTHER" }, { "name": "Blood sample for DNA analysis", "type": "GENETIC" }, { "name": "Stool sample for microbiome analysis", "type": "DIAGNOSTIC_TEST" }, { "name": "Mixed meal tolerance test", "type": "DIAGNOSTIC_TEST" }, { "name": "Continuous glucose monitoring", "type": "DIAGNOSTIC_TEST" }, { "name": "activity monitor", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "OTHER", "GENETIC", "DIAGNOSTIC_TEST" ], "sponsor": "Joslin Diabetes Center", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "70 Years", "sex": "ALL", "summary": "18 Years to 70 Years" }, "enrollment_count": 33, "start_date": "2020-08-11", "completion_date": "2026-12", "has_results": false, "last_update_posted_date": "2026-02-06", "last_synced_at": "2026-10-23T23:35:35.614Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT04428723" }, { "nct_id": "NCT03316183", "title": "Cerebral Monitor Guided Therapy on Cerebral Outcomes After Cardiac Surgery", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Cardiac Surgery", "Protein Metabolomics", "Cerebral Function", "Cardiopulmonary Bypass" ], "interventions": [ { "name": "Perioperative and postoperative management", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Washington", "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": "2021-12-01", "completion_date": "2025-12-01", "has_results": false, "last_update_posted_date": "2021-02-23", "last_synced_at": "2026-10-23T23:35:35.614Z", "location_count": 1, "location_summary": "Seattle, Washington", "locations": [ { "city": "Seattle", "state": "Washington" } ], "official_url": "https://clinicaltrials.gov/study/NCT03316183" }, { "nct_id": "NCT04319237", "title": "Axicabtagene Ciloleucel:Neurocognitive and Patient-Reported Outcomes", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Diffuse Large B Cell Lymphoma", "Transformed Lymphoma" ], "interventions": [ { "name": "Handgrip strength test", "type": "OTHER" }, { "name": "Neuropsychological Assessment - Wechsler Test of Adult Reading (WTAR)", "type": "BEHAVIORAL" }, { "name": "Neuropsychological Assessment - Repeatable Battery for the Assessment of Status (RBANS)", "type": "BEHAVIORAL" }, { "name": "Neuropsychological Assessment - Color Trails", "type": "BEHAVIORAL" }, { "name": "Neuropsychological Assessment -Stroop Color and Word Test", "type": "BEHAVIORAL" }, { "name": "Patient Reported Outcomes Measurement Information System-29 (PROMIS-29) Questionnaire", "type": "BEHAVIORAL" }, { "name": "European Organization for the Research and Treatment of Cancer Quality of Life Questionnaire", "type": "BEHAVIORAL" }, { "name": "Quality of Life (EQ-5D-5L) Questionnaire", "type": "BEHAVIORAL" }, { "name": "PROMIS Cognitive Function 4a Questionnaire", "type": "BEHAVIORAL" }, { "name": "Comprehensive Score for Financial Toxicity (COST) measure", "type": "BEHAVIORAL" } ], "intervention_types": [ "OTHER", "BEHAVIORAL" ], "sponsor": "H. Lee Moffitt Cancer Center and Research Institute", "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": "2020-03-10", "completion_date": "2023-07-31", "has_results": false, "last_update_posted_date": "2026-03-02", "last_synced_at": "2026-10-23T23:35:35.614Z", "location_count": 1, "location_summary": "Tampa, Florida", "locations": [ { "city": "Tampa", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT04319237" }, { "nct_id": "NCT07136272", "title": "Detection of Sleep Stages and Arousals Using Neural Network Classifiers", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Sleep Disordered Breathing (SDB)", "Sleep Apnea" ], "interventions": [ { "name": "SSAM", "type": "DEVICE" }, { "name": "Polysomnography", "type": "DIAGNOSTIC_TEST" }, { "name": "EnsoSleep", "type": "DEVICE" } ], "intervention_types": [ "DEVICE", "DIAGNOSTIC_TEST" ], "sponsor": "Pathway Medtech, LLC.", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 72, "start_date": "2025-10-04", "completion_date": "2025-12-21", "has_results": false, "last_update_posted_date": "2026-09-16", "last_synced_at": "2026-10-23T23:35:35.614Z", "location_count": 3, "location_summary": "Burlingame, California • Irvine, California • La Jolla, California", "locations": [ { "city": "Burlingame", "state": "California" }, { "city": "Irvine", "state": "California" }, { "city": "La Jolla", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT07136272" }, { "nct_id": "NCT01975363", "title": "Pilot Study of Curcumin for Women With Obesity and High Risk for Breast Cancer", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Atypical Ductal Breast Hyperplasia", "BRCA1 Gene Mutation", "BRCA2 Gene Mutation", "Ductal Breast Carcinoma in Situ", "Lobular Breast Carcinoma in Situ" ], "interventions": [ { "name": "curcumin", "type": "DIETARY_SUPPLEMENT" }, { "name": "Biomarker analysis", "type": "OTHER" }, { "name": "Assessment of Dietary Intake", "type": "OTHER" }, { "name": "Daily Log", "type": "OTHER" } ], "intervention_types": [ "DIETARY_SUPPLEMENT", "OTHER" ], "sponsor": "Ohio State University Comprehensive Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "19 Years", "maximum_age": null, "sex": "FEMALE", "summary": "19 Years and older · Female only" }, "enrollment_count": 29, "start_date": "2013-06", "completion_date": "2016-09-19", "has_results": false, "last_update_posted_date": "2019-08-30", "last_synced_at": "2026-10-23T23:35:35.614Z", "location_count": 1, "location_summary": "Columbus, Ohio", "locations": [ { "city": "Columbus", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT01975363" }, { "nct_id": "NCT06763549", "title": "COR-INSIGHT: Optimizing Cardiovascular and Cardiopulmonary Outcomes with AI-Driven Multiplexed Indications Using COR ECG Wearable", "overall_status": "ENROLLING_BY_INVITATION", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Cardiopulmonary Failure", "Myocardial Infarction (MI)", "Heart Decompensation", "Heart Failure", "HFrEF - Heart Failure with Reduced Ejection Fraction", "HFpEF - Heart Failure with Preserved Ejection Fraction", "Syncopation", "Syncope", "Ischemic Cardiovascular Disease", "STEMI", "STEMI (ST Elevation MI)", "Atrial Fibrillation (AF)", "Atrial Enlargement", "LVF", "Conduction Defect", "Conduction Abnormalities", "Heart Block", "Valvular Diseases", "Cardiac Output, Low", "Stroke Volume", "Stroke Volume Variation", "Hyperkalemia", "Hypercalcemia", "Hypocalcemia", "LV Dysfunction", "QT Prolongation", "Sudden Cardiac Death Due to Cardiac Arrhythmia", "Ventricular Arrhythmia", "Pacing", "Pacing Induced Dyssynchrony", "Silent Ischemia", "Pericarditis", "Sleep Related Breathing Disorder", "RSA", "Apnea, Obstructive", "Cardiac Output Measurement", "Respiratory Impedance", "CRT And/or ICD", "Infarction", "Cardiomyopathies, Primary", "Hypertrophy" ], "interventions": [ { "name": "SUBPROTOCOL A", "type": "DEVICE" }, { "name": "SUBPROTOCOL B", "type": "DEVICE" }, { "name": "SUBPROTOCOL C", "type": "DEVICE" }, { "name": "SUBPROTOCOL D", "type": "DEVICE" }, { "name": "SUBPROTOCOL E", "type": "DEVICE" }, { "name": "SUBPROTOCOL F", "type": "DEVICE" }, { "name": "SUBPROTOCOL G", "type": "DEVICE" }, { "name": "SUBPROTOCOL H", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Peerbridge Health, Inc", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 15000, "start_date": "2024-11-16", "completion_date": "2026-04-15", "has_results": false, "last_update_posted_date": "2025-01-08", "last_synced_at": "2026-10-23T23:35:35.614Z", "location_count": 1, "location_summary": "Melbourne, Florida", "locations": [ { "city": "Melbourne", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT06763549" }, { "nct_id": "NCT04733638", "title": "ADVANCE- Automated Detection and Volumetric Assessment of ICH", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Intracerebral Hemorrhage" ], "interventions": [ { "name": "Viz ICH VOLUME", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Viz.ai, Inc.", "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": "2021-01-26", "completion_date": "2023-04-28", "has_results": false, "last_update_posted_date": "2024-09-19", "last_synced_at": "2026-10-23T23:35:35.614Z", "location_count": 5, "location_summary": "Englewood, Colorado • New York, New York • Charlotte, North Carolina + 2 more", "locations": [ { "city": "Englewood", "state": "Colorado" }, { "city": "New York", "state": "New York" }, { "city": "Charlotte", "state": "North Carolina" }, { "city": "Winston-Salem", "state": "North Carolina" }, { "city": "Greenville", "state": "South Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT04733638" }, { "nct_id": "NCT07340853", "title": "CRISPR Delivered Anti-BCMA Car-T Therapy for Relapsed or Refractory Multiple Myeloma", "overall_status": "SUSPENDED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Multiple Myeloma", "Recurrent Multiple Myeloma", "Refractory Multiple Myeloma" ], "interventions": [ { "name": "Leukapheresis", "type": "PROCEDURE" }, { "name": "Cyclophosphamide", "type": "DRUG" }, { "name": "Chimeric Antigen Receptor T cells (CAR-T) Targeting BCMA", "type": "BIOLOGICAL" }, { "name": "Quality of Life (QoL) Questionnaires", "type": "BEHAVIORAL" }, { "name": "Bone Marrow Biopsy", "type": "PROCEDURE" }, { "name": "Biospecimen Collection", "type": "BIOLOGICAL" }, { "name": "Fludarabine", "type": "DRUG" }, { "name": "Radiographic imaging", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE", "DRUG", "BIOLOGICAL", "BEHAVIORAL" ], "sponsor": "Thomas Martin, MD", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 30, "start_date": "2026-02-28", "completion_date": "2043-05-25", "has_results": false, "last_update_posted_date": "2026-06-11", "last_synced_at": "2026-10-23T23:35:35.614Z", "location_count": 1, "location_summary": "San Francisco, California", "locations": [ { "city": "San Francisco", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT07340853" } ] }