{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Goals&page=7", "query": { "condition": "Goals", "page": 7 }, "page_size": 10 }, "pagination": { "page": 7, "page_size": 10, "total_count": 521, "total_pages": 53, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Goals&page=8&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Goals&page=6&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-21T23:14:27.156Z", "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": "NCT07273773", "title": "Evaluation of the Rigicon Infla10® Inflatable Penile Prosthesis (IPP) for Erectile Dysfunction", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Erectile Dysfunction (ED)" ], "interventions": [ { "name": "Rigicon Infla10® Inflatable Penile Prosthesis (IPP)", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Rigicon, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "22 Years", "maximum_age": null, "sex": "MALE", "summary": "22 Years and older · Male only" }, "enrollment_count": 182, "start_date": "2026-01-26", "completion_date": "2029-07", "has_results": false, "last_update_posted_date": "2026-08-13", "last_synced_at": "2026-10-21T23:14:27.156Z", "location_count": 4, "location_summary": "Coral Gables, Florida • Tampa, Florida • Atlanta, Georgia + 1 more", "locations": [ { "city": "Coral Gables", "state": "Florida" }, { "city": "Tampa", "state": "Florida" }, { "city": "Atlanta", "state": "Georgia" }, { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT07273773" }, { "nct_id": "NCT01082614", "title": "Arterial Pulse Waveform Contour Analysis for Intraoperative Goal Directed Therapy in Major Abdominal Surgery", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Surgical Procedures, Operative" ], "interventions": [ { "name": "Vigileo", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Loma Linda University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 46, "start_date": "2009-08", "completion_date": "2013-09", "has_results": true, "last_update_posted_date": "2019-03-26", "last_synced_at": "2026-10-21T23:14:27.156Z", "location_count": 1, "location_summary": "Loma Linda, California", "locations": [ { "city": "Loma Linda", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT01082614" }, { "nct_id": "NCT07615998", "title": "Young Adult Latino Testicular Cancer Survivors: a Pilot Study of Goal-Focused Emotion Regulation Therapy (GET)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Testicular Cancer" ], "interventions": [ { "name": "Goal-focused Emotion-regulation Therapy", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of California, Irvine", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "39 Years", "sex": "MALE", "summary": "18 Years to 39 Years · Male only" }, "enrollment_count": 35, "start_date": "2020-08-05", "completion_date": "2023-08-14", "has_results": false, "last_update_posted_date": "2026-05-29", "last_synced_at": "2026-10-21T23:14:27.156Z", "location_count": 1, "location_summary": "Irvine, California", "locations": [ { "city": "Irvine", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT07615998" }, { "nct_id": "NCT04579614", "title": "Performance Feedback in Health Care", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Influenza" ], "interventions": [ { "name": "The Impact of Performance Feedback and Variable Goal Setting on Flu Vaccination Success Rates of Providers", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Kaiser Permanente", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 595, "start_date": "2019-09-23", "completion_date": "2019-12-31", "has_results": false, "last_update_posted_date": "2020-10-08", "last_synced_at": "2026-10-21T23:14:27.156Z", "location_count": 1, "location_summary": "Atlanta, Georgia", "locations": [ { "city": "Atlanta", "state": "Georgia" } ], "official_url": "https://clinicaltrials.gov/study/NCT04579614" }, { "nct_id": "NCT00692471", "title": "Sleep Actigraphy in Postural Tachycardia Syndrome (POTS)", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Postural Tachycardia Syndrome", "Orthostatic Intolerance", "Sleep Disorders" ], "interventions": [ { "name": "Actigraphy Watch (motion sensors) with light sensors - ActiWatch from Minimitter", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Satish R. Raj", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "18 Years to 65 Years" }, "enrollment_count": 100, "start_date": "2008-06", "completion_date": "2029-12", "has_results": false, "last_update_posted_date": "2026-10-16", "last_synced_at": "2026-10-21T23:14:27.156Z", "location_count": 1, "location_summary": "Nashville, Tennessee", "locations": [ { "city": "Nashville", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT00692471" }, { "nct_id": "NCT07652359", "title": "Empowering Monterey Bay Residents for Activated, Collaborative, and Equitable Care", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Shared Decision-Making", "Quality of Life", "Advanced Illness", "Terminal Illness" ], "interventions": [ { "name": "Research Assistant Support", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Stanford University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 138, "start_date": "2026-08-26", "completion_date": "2030-01-14", "has_results": false, "last_update_posted_date": "2026-08-27", "last_synced_at": "2026-10-21T23:14:27.156Z", "location_count": 1, "location_summary": "Palo Alto, California", "locations": [ { "city": "Palo Alto", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT07652359" }, { "nct_id": "NCT01714531", "title": "Improving Outcomes After Traumatic Injury: A Goal Management Approach", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Traumatic Brain Injury" ], "interventions": [ { "name": "Telephone-Based Goal Management Training", "type": "BEHAVIORAL" }, { "name": "Telephone-Based Attention-Control", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Vanderbilt University Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "21 Years to 80 Years" }, "enrollment_count": 91, "start_date": "2013-01", "completion_date": "2016-09", "has_results": false, "last_update_posted_date": "2017-04-24", "last_synced_at": "2026-10-21T23:14:27.156Z", "location_count": 1, "location_summary": "Nashville, Tennessee", "locations": [ { "city": "Nashville", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT01714531" }, { "nct_id": "NCT02407496", "title": "Neurophysiological Attention Test (NAT) for Objective Assessment of Attention Deficit Hyperactivity Disorder (ADHD)", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Attention Deficit Hyperactivity Disorder (ADHD)" ], "interventions": [ { "name": "Behavioral assessment and NAT EEG tests", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Think Now Incorporated", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "40 Years", "sex": "ALL", "summary": "18 Years to 40 Years" }, "enrollment_count": 80, "start_date": "2014-06", "completion_date": "2015-09", "has_results": false, "last_update_posted_date": "2020-12-10", "last_synced_at": "2026-10-21T23:14:27.156Z", "location_count": 1, "location_summary": "Los Angeles, California", "locations": [ { "city": "Los Angeles", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT02407496" }, { "nct_id": "NCT00284167", "title": "Efficacy of a Web-based Tailored Weight Management Program", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2", "PHASE3" ], "conditions": [ "Obesity" ], "interventions": [ { "name": "tailored web-based weight management intervention", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Robert Wood Johnson Foundation", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "18 Years to 75 Years" }, "enrollment_count": 1848, "start_date": "2003-09", "completion_date": "2006-07", "has_results": false, "last_update_posted_date": "2011-07-27", "last_synced_at": "2026-10-21T23:14:27.156Z", "location_count": 1, "location_summary": "Walnut Creek, California", "locations": [ { "city": "Walnut Creek", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT00284167" }, { "nct_id": "NCT00554944", "title": "Intraoperative Goal-directed Fluid Management", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Obesity", "Abdominal Surgery", "Hysterectomy", "Genital Prolapse" ], "interventions": [ { "name": "Esophageal probe", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "The Cleveland Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "85 Years", "sex": "ALL", "summary": "18 Years to 85 Years" }, "enrollment_count": 0, "start_date": "2007-06", "completion_date": "2010-02", "has_results": false, "last_update_posted_date": "2017-01-23", "last_synced_at": "2026-10-21T23:14:27.156Z", "location_count": 1, "location_summary": "Cleveland, Ohio", "locations": [ { "city": "Cleveland", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT00554944" } ] }