{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Neurologic+Examination", "query": { "intervention": "Neurologic Examination" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 484, "total_pages": 49, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Neurologic+Examination&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-09-02T05:41:58.692Z", "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": "NCT01066325", "title": "Improving Flexibility With a Mindbody Approach", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "EARLY_PHASE1" ], "conditions": [ "General Low Back Hip and Hamstring Flexibility" ], "interventions": [ { "name": "Neuro Emotional Technique", "type": "BEHAVIORAL" }, { "name": "Stretching Instruction", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "Parker Research Institute", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "45 Years", "sex": "FEMALE", "summary": "18 Years to 45 Years · Female only" }, "enrollment_count": 45, "start_date": "2010-03", "completion_date": "2010-08", "has_results": false, "last_update_posted_date": "2017-06-20", "last_synced_at": "2026-09-02T05:41:58.692Z", "location_count": 1, "location_summary": "Dallas, Texas", "locations": [ { "city": "Dallas", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT01066325" }, { "nct_id": "NCT01485731", "title": "Safety Study of Nelfinavir + Cisplatin + Pelvic Radiation Therapy to Treat Cervical Cancer", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Cervical Cancer" ], "interventions": [ { "name": "Nelfinavir", "type": "DRUG" }, { "name": "Cisplatin", "type": "DRUG" }, { "name": "Pelvic External Beam Radiation Therapy", "type": "RADIATION" }, { "name": "Brachytherapy", "type": "RADIATION" }, { "name": "Pharmacokinetic Sampling", "type": "PROCEDURE" }, { "name": "Cervical Biopsy", "type": "PROCEDURE" }, { "name": "Pelvic Examination", "type": "PROCEDURE" }, { "name": "Pap Smear", "type": "PROCEDURE" }, { "name": "Audiogram", "type": "PROCEDURE" }, { "name": "Proctoscopy", "type": "PROCEDURE" }, { "name": "Cytoscopy", "type": "PROCEDURE" }, { "name": "Renal Ultrasound", "type": "PROCEDURE" }, { "name": "CT Scan", "type": "PROCEDURE" }, { "name": "Whole Body PET/CT Scan", "type": "PROCEDURE" } ], "intervention_types": [ "DRUG", "RADIATION", "PROCEDURE" ], "sponsor": "University of Miami", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 8, "start_date": "2012-01", "completion_date": "2015-02", "has_results": false, "last_update_posted_date": "2015-06-03", "last_synced_at": "2026-09-02T05:41:58.692Z", "location_count": 1, "location_summary": "Miami, Florida", "locations": [ { "city": "Miami", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT01485731" }, { "nct_id": "NCT06038175", "title": "vHIT Testing for Presentation of Dizziness at a Comprehensive Stroke Center", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Stroke, Acute", "Vertigo", "Vertigo, Peripheral", "Dizziness", "Dizziness; Syndrome" ], "interventions": [ { "name": "Video Head Impulse Testing", "type": "DEVICE" }, { "name": "Standard of care neurologic evaluation", "type": "OTHER" } ], "intervention_types": [ "DEVICE", "OTHER" ], "sponsor": "Medical University of South Carolina", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "90 Years", "sex": "ALL", "summary": "18 Years to 90 Years" }, "enrollment_count": 30, "start_date": "2024-01-16", "completion_date": "2024-07-31", "has_results": false, "last_update_posted_date": "2024-08-26", "last_synced_at": "2026-09-02T05:41:58.692Z", "location_count": 1, "location_summary": "Charleston, South Carolina", "locations": [ { "city": "Charleston", "state": "South Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT06038175" }, { "nct_id": "NCT04269239", "title": "Effectiveness of Healthy Habits for Hospitalized Older Adults to Optimize Rehabilitation", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Insomnia", "Pain", "Osteoarthritis, Knee", "Osteoarthritis, Hip" ], "interventions": [ { "name": "Healthy Habits", "type": "BEHAVIORAL" }, { "name": "Sleep Habits", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Baylor College of Medicine", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "40 Years", "maximum_age": null, "sex": "ALL", "summary": "40 Years and older" }, "enrollment_count": 73, "start_date": "2021-04-30", "completion_date": "2024-11-30", "has_results": true, "last_update_posted_date": "2026-09-01", "last_synced_at": "2026-09-02T05:41:58.692Z", "location_count": 3, "location_summary": "Galveston, Texas • Houston, Texas", "locations": [ { "city": "Galveston", "state": "Texas" }, { "city": "Houston", "state": "Texas" }, { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT04269239" }, { "nct_id": "NCT02603692", "title": "Health Related Quality of Life in Pediatric Central Nervous System (CNS) Tumors: A Feasibility Study Utilizing PROMIS", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Brain Neoplasms" ], "interventions": [ { "name": "PROMIS-QOL", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Children's Hospital Medical Center, Cincinnati", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "5 Years", "maximum_age": "35 Years", "sex": "ALL", "summary": "5 Years to 35 Years" }, "enrollment_count": 20, "start_date": "2014-11", "completion_date": "2018-10", "has_results": false, "last_update_posted_date": "2019-07-11", "last_synced_at": "2026-09-02T05:41:58.692Z", "location_count": 1, "location_summary": "Cincinnati, Ohio", "locations": [ { "city": "Cincinnati", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT02603692" }, { "nct_id": "NCT07466316", "title": "A Study Comparing Higher Dose Chemotherapy Over a Shorter Amount of Time to Lower Dose Chemotherapy Plus Maintenance Over a Longer Amount of Time in Patients With Newly Diagnosed Intermediate-Risk Rhabdomyosarcoma (IR RMS)", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Rhabdomyosarcoma" ], "interventions": [ { "name": "Biospecimen Collection", "type": "PROCEDURE" }, { "name": "Bone Marrow Aspiration", "type": "PROCEDURE" }, { "name": "Bone Marrow Biopsy", "type": "PROCEDURE" }, { "name": "Bone Scan", "type": "PROCEDURE" }, { "name": "Computed Tomography", "type": "PROCEDURE" }, { "name": "Cyclophosphamide", "type": "DRUG" }, { "name": "Dactinomycin", "type": "BIOLOGICAL" }, { "name": "Irinotecan Hydrochloride", "type": "DRUG" }, { "name": "Lumbar Puncture", "type": "PROCEDURE" }, { "name": "Lymph Node Biopsy", "type": "PROCEDURE" }, { "name": "Magnetic Resonance Imaging", "type": "PROCEDURE" }, { "name": "Positron Emission Tomography", "type": "PROCEDURE" }, { "name": "Radiation Therapy", "type": "RADIATION" }, { "name": "Resection", "type": "PROCEDURE" }, { "name": "Survey Administration", "type": "OTHER" }, { "name": "Vincristine Sulfate", "type": "DRUG" }, { "name": "Vinorelbine Tartrate", "type": "DRUG" } ], "intervention_types": [ "PROCEDURE", "DRUG", "BIOLOGICAL", "RADIATION", "OTHER" ], "sponsor": "Children's Oncology Group", "sponsor_class": "NETWORK", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": "50 Years", "sex": "ALL", "summary": "Up to 50 Years" }, "enrollment_count": 342, "start_date": "2026-07-14", "completion_date": "2031-03-31", "has_results": false, "last_update_posted_date": "2026-08-25", "last_synced_at": "2026-09-02T05:41:58.692Z", "location_count": 86, "location_summary": "Birmingham, Alabama • Mobile, Alabama • Little Rock, Arkansas + 71 more", "locations": [ { "city": "Birmingham", "state": "Alabama" }, { "city": "Mobile", "state": "Alabama" }, { "city": "Little Rock", "state": "Arkansas" }, { "city": "Duarte", "state": "California" }, { "city": "Loma Linda", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT07466316" }, { "nct_id": "NCT05513274", "title": "Heartache and Backache- An Online Intervention Addressing Emotional and Physical Pain", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Chronic Pain (Back / Neck)" ], "interventions": [ { "name": "Pain Psychology Neuroscience + Written Emotional Disclosure", "type": "BEHAVIORAL" }, { "name": "Pain Psychology Neuroscience + Healthy Habits Disclosure", "type": "BEHAVIORAL" }, { "name": "Health Behavior Control + Written Emotional Disclosure", "type": "BEHAVIORAL" }, { "name": "Health Behavior Control + Healthy Habits Disclosure", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Wayne State University", "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": 107, "start_date": "2022-12-15", "completion_date": "2024-12-30", "has_results": false, "last_update_posted_date": "2025-07-16", "last_synced_at": "2026-09-02T05:41:58.692Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT05513274" }, { "nct_id": "NCT06945835", "title": "High Intensity Exercise and Improving Physical Activity Among People With Neurologic Dysfunction", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Cerebral Palsy (CP)", "Stroke", "Spinal Cord Injury", "Traumatic Brain Injury", "Charcot Marie Tooth Disease (CMT)", "Spina Bifida" ], "interventions": [ { "name": "Participate in high intensity exercise of at least 20 minutes in 60 minutes session of RPE greater than 6.", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Hartford", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "8 Years", "maximum_age": "99 Years", "sex": "ALL", "summary": "8 Years to 99 Years" }, "enrollment_count": 15, "start_date": "2025-02-24", "completion_date": "2025-05-27", "has_results": false, "last_update_posted_date": "2025-11-03", "last_synced_at": "2026-09-02T05:41:58.692Z", "location_count": 1, "location_summary": "West Hartford, Connecticut", "locations": [ { "city": "West Hartford", "state": "Connecticut" } ], "official_url": "https://clinicaltrials.gov/study/NCT06945835" }, { "nct_id": "NCT00064623", "title": "Study of NGX-4010 for the Treatment of Painful HIV-Associated Neuropathy", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "HIV Infections", "Peripheral Nervous System Diseases", "Pain" ], "interventions": [ { "name": "Capsaicin Dermal Patch", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "NeurogesX", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 300, "start_date": "2003-08", "completion_date": "2005-11", "has_results": false, "last_update_posted_date": "2008-03-06", "last_synced_at": "2026-09-02T05:41:58.692Z", "location_count": 35, "location_summary": "Phoenix, Arizona • Berkeley, California • San Diego, California + 29 more", "locations": [ { "city": "Phoenix", "state": "Arizona" }, { "city": "Phoenix", "state": "Arizona" }, { "city": "Berkeley", "state": "California" }, { "city": "San Diego", "state": "California" }, { "city": "San Francisco", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT00064623" }, { "nct_id": "NCT05086159", "title": "Effectiveness of Pain Neuroscience Education (PNE) to Veterans With Post-Traumatic Stress and Low Back Pain", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Chronic Low Back Pain", "Post-traumatic Stress" ], "interventions": [ { "name": "Pain Neuroscience Education", "type": "BEHAVIORAL" }, { "name": "Exercise", "type": "BEHAVIORAL" }, { "name": "Traditional Education", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Keller Army Community Hospital", "sponsor_class": "FED", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "18 Years to 65 Years" }, "enrollment_count": 47, "start_date": "2017-07-01", "completion_date": "2021-08-01", "has_results": false, "last_update_posted_date": "2021-10-27", "last_synced_at": "2026-09-02T05:41:58.692Z", "location_count": 1, "location_summary": "Lexington, Kentucky", "locations": [ { "city": "Lexington", "state": "Kentucky" } ], "official_url": "https://clinicaltrials.gov/study/NCT05086159" } ] }