{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Sensitivity+Intervention&page=10", "query": { "intervention": "Sensitivity Intervention", "page": 10 }, "page_size": 10 }, "pagination": { "page": 10, "page_size": 10, "total_count": 756, "total_pages": 76, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Sensitivity+Intervention&page=11&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Sensitivity+Intervention&page=9&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-20T01:03:27.560Z", "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": "NCT00875225", "title": "Using Multimedia Technology for Hypertension Control for Low-Income African Americans", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Hypertension" ], "interventions": [ { "name": "DVD", "type": "BEHAVIORAL" }, { "name": "Intervention DVD", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Cooper Green Mercy Hospital", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 300, "start_date": "2006-12", "completion_date": "2009-05", "has_results": false, "last_update_posted_date": "2009-04-03", "last_synced_at": "2026-10-20T01:03:27.560Z", "location_count": 1, "location_summary": "Birmingham, Alabama", "locations": [ { "city": "Birmingham", "state": "Alabama" } ], "official_url": "https://clinicaltrials.gov/study/NCT00875225" }, { "nct_id": "NCT01127659", "title": "Testosterone Replacement in Men With Diabetes and Obesity", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Hypogonadism" ], "interventions": [ { "name": "testosterone", "type": "DRUG" }, { "name": "placebo", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "University at Buffalo", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "30 Years", "maximum_age": "65 Years", "sex": "MALE", "summary": "30 Years to 65 Years · Male only" }, "enrollment_count": 137, "start_date": "2010-05", "completion_date": "2015-11", "has_results": true, "last_update_posted_date": "2022-11-29", "last_synced_at": "2026-10-20T01:03:27.560Z", "location_count": 1, "location_summary": "Williamsville, New York", "locations": [ { "city": "Williamsville", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT01127659" }, { "nct_id": "NCT00004153", "title": "Detection of Melanoma Markers in Lymph Nodes or Peripheral Blood of Patients With Melanoma", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Melanoma (Skin)" ], "interventions": [ { "name": "reverse transcriptase-polymerase chain reaction", "type": "GENETIC" }, { "name": "sentinel lymph node biopsy", "type": "PROCEDURE" } ], "intervention_types": [ "GENETIC", "PROCEDURE" ], "sponsor": "University of Chicago", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 106, "start_date": "1998-06", "completion_date": "2005-01", "has_results": false, "last_update_posted_date": "2013-09-05", "last_synced_at": "2026-10-20T01:03:27.560Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT00004153" }, { "nct_id": "NCT07793539", "title": "Understanding Information Preferences, Risk Perceptions, and Tradeoffs When Making Decisions About Multi-cancer Early Detection Tests", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Early Detection of Cancer" ], "interventions": [ { "name": "Test Performance Information: High Detail", "type": "BEHAVIORAL" }, { "name": "Test Performance Information: Low Detail", "type": "BEHAVIORAL" }, { "name": "Diagnostic Workup Information: High Detail", "type": "BEHAVIORAL" }, { "name": "Diagnostic Workup Information: Low Detail", "type": "BEHAVIORAL" }, { "name": "Test and Workup Cost Information: High Detail", "type": "BEHAVIORAL" }, { "name": "Test and Workup Cost Information: Low Detail", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Trustees of Dartmouth College", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "40 Years", "maximum_age": "74 Years", "sex": "ALL", "summary": "40 Years to 74 Years" }, "enrollment_count": 3000, "start_date": "2027-09", "completion_date": "2029-07", "has_results": false, "last_update_posted_date": "2026-08-28", "last_synced_at": "2026-10-20T01:03:27.560Z", "location_count": 1, "location_summary": "Lebanon, New Hampshire", "locations": [ { "city": "Lebanon", "state": "New Hampshire" } ], "official_url": "https://clinicaltrials.gov/study/NCT07793539" }, { "nct_id": "NCT03862222", "title": "Atlas of Retinal Imaging in Alzheimer's Study", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Alzheimer Disease", "Mild Cognitive Impairment", "Mild Dementia", "Aging", "Cognitive Change" ], "interventions": [ { "name": "Retinal Imaging", "type": "OTHER" }, { "name": "Pupillometry", "type": "OTHER" }, { "name": "Contrast Sensitivity", "type": "OTHER" }, { "name": "Neuropsychological Evaluation", "type": "DIAGNOSTIC_TEST" }, { "name": "APOE genotyping", "type": "GENETIC" }, { "name": "blood draw", "type": "OTHER" }, { "name": "Gait Assessment", "type": "OTHER" }, { "name": "Actigraphy", "type": "OTHER" } ], "intervention_types": [ "OTHER", "DIAGNOSTIC_TEST", "GENETIC" ], "sponsor": "University of Rhode Island", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "55 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "55 Years to 80 Years" }, "enrollment_count": 165, "start_date": "2019-12-16", "completion_date": "2025-05-31", "has_results": false, "last_update_posted_date": "2025-06-05", "last_synced_at": "2026-10-20T01:03:27.560Z", "location_count": 4, "location_summary": "Clearwater, Florida • St. Petersburg, Florida • Kingston, Rhode Island + 1 more", "locations": [ { "city": "Clearwater", "state": "Florida" }, { "city": "St. Petersburg", "state": "Florida" }, { "city": "Kingston", "state": "Rhode Island" }, { "city": "Providence", "state": "Rhode Island" } ], "official_url": "https://clinicaltrials.gov/study/NCT03862222" }, { "nct_id": "NCT01529151", "title": "Effectiveness of Osteopathic Manipulative Treatment (OMT) and Vestibular Rehabilitation Therapy (VRT) in Individuals With Vertigo", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Vertigo", "Dizziness", "Benign Paroxysmal Positional Vertigo", "Labyrinthitis" ], "interventions": [ { "name": "Osteopathic Manipulative Treatment (OMT)", "type": "OTHER" }, { "name": "Vestibular Rehabilitation Therapy (VRT)", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Western University of Health Sciences", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "79 Years", "sex": "ALL", "summary": "18 Years to 79 Years" }, "enrollment_count": 26, "start_date": "2012-01", "completion_date": "2014-08", "has_results": false, "last_update_posted_date": "2015-06-10", "last_synced_at": "2026-10-20T01:03:27.560Z", "location_count": 1, "location_summary": "Pomona, California", "locations": [ { "city": "Pomona", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT01529151" }, { "nct_id": "NCT07180446", "title": "Can Gut Bacteria Predict Who Benefits Most From Exercise? A Gut Supplement to Help Exercise Non-Responders", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Obesity &Amp; Overweight" ], "interventions": [ { "name": "Cardiovascular Exercise", "type": "BEHAVIORAL" }, { "name": "Butyrate", "type": "DIETARY_SUPPLEMENT" } ], "intervention_types": [ "BEHAVIORAL", "DIETARY_SUPPLEMENT" ], "sponsor": "Texas Christian University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "40 Years", "sex": "FEMALE", "summary": "18 Years to 40 Years · Female only" }, "enrollment_count": 40, "start_date": "2026-01-18", "completion_date": "2027-04-30", "has_results": false, "last_update_posted_date": "2026-09-29", "last_synced_at": "2026-10-20T01:03:27.560Z", "location_count": 1, "location_summary": "Fort Worth, Texas", "locations": [ { "city": "Fort Worth", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT07180446" }, { "nct_id": "NCT00673569", "title": "Laboratory Test in Predicting Response to Erlotinib in Patients With Relapsed Metastatic or Unresectable Non-Small Cell Lung Cancer That Did Not Respond to Previous Treatment", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Lung Cancer" ], "interventions": [ { "name": "erlotinib hydrochloride", "type": "DRUG" }, { "name": "gene expression analysis", "type": "GENETIC" }, { "name": "protein expression analysis", "type": "GENETIC" }, { "name": "immunoenzyme technique", "type": "OTHER" }, { "name": "immunologic technique", "type": "OTHER" }, { "name": "laboratory biomarker analysis", "type": "OTHER" }, { "name": "needle biopsy", "type": "PROCEDURE" } ], "intervention_types": [ "DRUG", "GENETIC", "OTHER", "PROCEDURE" ], "sponsor": "Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 40, "start_date": "2006-09", "completion_date": null, "has_results": false, "last_update_posted_date": "2010-08-09", "last_synced_at": "2026-10-20T01:03:27.560Z", "location_count": 1, "location_summary": "Baltimore, Maryland", "locations": [ { "city": "Baltimore", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT00673569" }, { "nct_id": "NCT02647463", "title": "Evaluating the Efficacy of ABC for High-Risk Parent and Infants", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Attachment Disorders" ], "interventions": [ { "name": "Attachment and Biobehavioral Catch-up (ABC)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Stony Brook University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "6 Months", "maximum_age": "20 Months", "sex": "ALL", "summary": "6 Months to 20 Months" }, "enrollment_count": 200, "start_date": "2016-01", "completion_date": "2018-10", "has_results": false, "last_update_posted_date": "2018-04-18", "last_synced_at": "2026-10-20T01:03:27.560Z", "location_count": 1, "location_summary": "Brooklyn, New York", "locations": [ { "city": "Brooklyn", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT02647463" }, { "nct_id": "NCT03951064", "title": "Providing Optimal PEEP During Mechanical Ventilation for Obese Patients Using Esophageal Balloon", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Obesity, Morbid", "Ventilator-Induced Lung Injury", "Respiratory Failure" ], "interventions": [ { "name": "Esophageal balloon", "type": "DEVICE" }, { "name": "Intervention Spontaneous Breathing Trial (SBT) and Extubation", "type": "PROCEDURE" }, { "name": "Control Spontaneous Breathing Trial and Extubation", "type": "PROCEDURE" }, { "name": "Intervention Weaning after Tracheostomy", "type": "PROCEDURE" }, { "name": "Control Weaning after Tracheostomy", "type": "PROCEDURE" } ], "intervention_types": [ "DEVICE", "PROCEDURE" ], "sponsor": "University of North Carolina, Chapel Hill", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 6, "start_date": "2021-03-31", "completion_date": "2022-12-06", "has_results": true, "last_update_posted_date": "2024-06-05", "last_synced_at": "2026-10-20T01:03:27.560Z", "location_count": 2, "location_summary": "Chapel Hill, North Carolina • Greenville, North Carolina", "locations": [ { "city": "Chapel Hill", "state": "North Carolina" }, { "city": "Greenville", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT03951064" } ] }