{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Videofluoroscopic+swallow+evaluation", "query": { "intervention": "Videofluoroscopic swallow evaluation" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 18, "total_pages": 2, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Videofluoroscopic+swallow+evaluation&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-09-07T08:26:27.431Z", "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": "NCT02003287", "title": "Comparing FEES to VFSS in Diagnosing Laryngeal Penetration and Aspiration in Infants in the NICU", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Deglutition Disorders" ], "interventions": [ { "name": "VFSS", "type": "OTHER" }, { "name": "FEES", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Baylor Research Institute", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "37 Weeks", "maximum_age": null, "sex": "ALL", "summary": "37 Weeks and older" }, "enrollment_count": 25, "start_date": "2013-11", "completion_date": "2014-10", "has_results": false, "last_update_posted_date": "2015-03-06", "last_synced_at": "2026-09-07T08:26:27.431Z", "location_count": 1, "location_summary": "Dallas, Texas", "locations": [ { "city": "Dallas", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT02003287" }, { "nct_id": "NCT04359199", "title": "QUantitative Assessment of Swallowing After Radiation (QUASAR)", "overall_status": "UNKNOWN", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Head and Neck Cancer", "Dysphagia", "Oropharyngeal Dysphagia", "Oropharynx Cancer", "Oropharynx Squamous Cell Carcinoma" ], "interventions": [ { "name": "Radiation Therapy", "type": "RADIATION" }, { "name": "Cetuximab", "type": "DRUG" }, { "name": "Chemotherapy", "type": "DRUG" }, { "name": "Immunotherapy", "type": "DRUG" } ], "intervention_types": [ "RADIATION", "DRUG" ], "sponsor": "Loren Mell, MD", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 42, "start_date": "2020-09-01", "completion_date": "2024-12-31", "has_results": false, "last_update_posted_date": "2023-02-10", "last_synced_at": "2026-09-07T08:26:27.431Z", "location_count": 2, "location_summary": "La Jolla, California", "locations": [ { "city": "La Jolla", "state": "California" }, { "city": "La Jolla", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT04359199" }, { "nct_id": "NCT02390089", "title": "Cough According to Stimulus Type in PD", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Parkinson's Disease" ], "interventions": [ { "name": "Capsaicin vapor", "type": "DRUG" }, { "name": "fog", "type": "OTHER" }, { "name": "Videofluoroscopic swallow evaluation", "type": "RADIATION" }, { "name": "Nebulizer", "type": "DEVICE" } ], "intervention_types": [ "DRUG", "OTHER", "RADIATION", "DEVICE" ], "sponsor": "University of Florida", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "50 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "50 Years to 80 Years" }, "enrollment_count": 158, "start_date": "2015-04", "completion_date": "2019-02-13", "has_results": false, "last_update_posted_date": "2019-02-15", "last_synced_at": "2026-09-07T08:26:27.431Z", "location_count": 1, "location_summary": "Gainesville, Florida", "locations": [ { "city": "Gainesville", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT02390089" }, { "nct_id": "NCT03122145", "title": "Normal Breathing and Swallowing in Healthy Volunteers", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1", "PHASE2" ], "conditions": [ "Healthy" ], "interventions": [ { "name": "Capsaicin", "type": "DRUG" }, { "name": "Videofluoroscopic swallow study", "type": "DEVICE" } ], "intervention_types": [ "DRUG", "DEVICE" ], "sponsor": "University of Florida", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "100 Years", "sex": "ALL", "summary": "18 Years to 100 Years" }, "enrollment_count": 49, "start_date": "2017-05-23", "completion_date": "2019-02-28", "has_results": true, "last_update_posted_date": "2021-01-14", "last_synced_at": "2026-09-07T08:26:27.431Z", "location_count": 1, "location_summary": "Gainesville, Florida", "locations": [ { "city": "Gainesville", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT03122145" }, { "nct_id": "NCT02710162", "title": "Accurate Screening Tools for Dysphagia in Amyotrophic Lateral Sclerosis (ALS)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "EARLY_PHASE1" ], "conditions": [ "Amyotrophic Lateral Sclerosis" ], "interventions": [ { "name": "Micro Mouth Pressure Meter", "type": "DEVICE" }, { "name": "Iowa Oral Performance Instrument", "type": "DEVICE" }, { "name": "Electrical Impedance Myography", "type": "DEVICE" }, { "name": "Capsaicin", "type": "DRUG" }, { "name": "Videofluoroscopic Swallowing Study", "type": "PROCEDURE" }, { "name": "Pulmonary Function Testing", "type": "PROCEDURE" }, { "name": "Swallowing Related Quality of Life Questionnaire", "type": "OTHER" }, { "name": "Functional Oral Intake Scale", "type": "OTHER" }, { "name": "Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised", "type": "OTHER" }, { "name": "Eating Assessment Tool-10", "type": "OTHER" }, { "name": "Communicative Effectiveness Survey", "type": "OTHER" }, { "name": "The Center for Neurologic Studies Bulbar Function Scale", "type": "OTHER" } ], "intervention_types": [ "DEVICE", "DRUG", "PROCEDURE", "OTHER" ], "sponsor": "University of Florida", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": "85 Years", "sex": "ALL", "summary": "21 Years to 85 Years" }, "enrollment_count": 21, "start_date": "2016-04", "completion_date": "2017-12-19", "has_results": false, "last_update_posted_date": "2017-12-21", "last_synced_at": "2026-09-07T08:26:27.431Z", "location_count": 1, "location_summary": "Gainesville, Florida", "locations": [ { "city": "Gainesville", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT02710162" }, { "nct_id": "NCT04773184", "title": "Improving Diagnostic Standards in Dysphagia", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Dysphagia" ], "interventions": [ { "name": "Fiberoptic Endoscopic Evaluation of Swallowing", "type": "PROCEDURE" }, { "name": "Videofluoroscopic Swallowing Study", "type": "PROCEDURE" }, { "name": "Voluntary Peak Cough Flow Testing", "type": "PROCEDURE" }, { "name": "Iowa Oral Performance Instrument", "type": "PROCEDURE" }, { "name": "Capsaicin Challenge", "type": "PROCEDURE" }, { "name": "Pulmonary Function Testing", "type": "PROCEDURE" }, { "name": "Voicing Tasks", "type": "OTHER" } ], "intervention_types": [ "PROCEDURE", "OTHER" ], "sponsor": "University of Florida", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "90 Years", "sex": "ALL", "summary": "18 Years to 90 Years" }, "enrollment_count": 46, "start_date": "2021-04-27", "completion_date": "2023-09-23", "has_results": false, "last_update_posted_date": "2024-01-17", "last_synced_at": "2026-09-07T08:26:27.431Z", "location_count": 1, "location_summary": "Gainesville, Florida", "locations": [ { "city": "Gainesville", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT04773184" }, { "nct_id": "NCT05304416", "title": "Clinical Markers of Dysphagia in Cardiac Surgical Patients", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Cardiovascular Diseases", "Dysphagia" ], "interventions": [ { "name": "Fiberoptic Endoscopic Evaluation of Swallowing", "type": "DIAGNOSTIC_TEST" }, { "name": "Simultaneous FEES and Videofluoroscopy instrumental swallowing exam", "type": "DIAGNOSTIC_TEST" }, { "name": "Videofluoroscopy instrumental swallowing exam (VFSS)", "type": "DIAGNOSTIC_TEST" }, { "name": "Voluntary Cough Peak Expiratory Flow (PEF) Testing", "type": "OTHER" }, { "name": "Reflex Cough Screen", "type": "OTHER" }, { "name": "Lingual Pressure Testing", "type": "OTHER" }, { "name": "Speech Testing", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "DIAGNOSTIC_TEST", "OTHER" ], "sponsor": "University of Florida", "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": 347, "start_date": "2022-06-07", "completion_date": "2026-12-31", "has_results": false, "last_update_posted_date": "2026-08-06", "last_synced_at": "2026-09-07T08:26:27.431Z", "location_count": 2, "location_summary": "Gainesville, Florida • Columbus, Ohio", "locations": [ { "city": "Gainesville", "state": "Florida" }, { "city": "Columbus", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT05304416" }, { "nct_id": "NCT05173207", "title": "Respiratory-Swallow Coordination in Cardiothoracic Surgical Patients", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Thoracic Diseases", "Cardiovascular Diseases" ], "interventions": [ { "name": "Videofluoroscopic swallow exam with concurrent monitoring of respiratory-swallow coordination", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "DIAGNOSTIC_TEST" ], "sponsor": "University of Florida", "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": 8, "start_date": "2022-03-03", "completion_date": "2022-07-27", "has_results": false, "last_update_posted_date": "2022-07-28", "last_synced_at": "2026-09-07T08:26:27.431Z", "location_count": 1, "location_summary": "Gainesville, Florida", "locations": [ { "city": "Gainesville", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT05173207" }, { "nct_id": "NCT04920344", "title": "Swallowing Outcomes and Circulating Tumor DNA in Patients With HPV Related Oropharyngeal Cancer Treated With Transoral Surgery and Reduced Intensity Adjuvant Therapy", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Clinical Stage I HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8", "Clinical Stage II HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8", "Clinical Stage III HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8", "Oropharyngeal Human Papillomavirus-Positive Squamous Cell Carcinoma" ], "interventions": [ { "name": "Transoral Surgery", "type": "PROCEDURE" }, { "name": "External Beam Radiation Therapy", "type": "RADIATION" }, { "name": "Cisplatin", "type": "DRUG" }, { "name": "Incisional Tumor Biopsy", "type": "PROCEDURE" }, { "name": "Circulating tumor deoxyribonucleic acid (ctDNA) levels assessment", "type": "OTHER" }, { "name": "MD Anderson Dysphagia Index", "type": "OTHER" }, { "name": "University of Washington Quality of Life Questionnaire", "type": "OTHER" }, { "name": "Euro-QOL 5 dimension scale questionnaire", "type": "OTHER" }, { "name": "Modified barium swallow (MBS) evaluation with aspiration-penetration scale", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "PROCEDURE", "RADIATION", "DRUG", "OTHER", "DIAGNOSTIC_TEST" ], "sponsor": "Rutgers, The State University of New Jersey", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 15, "start_date": "2021-05-19", "completion_date": "2026-09", "has_results": false, "last_update_posted_date": "2026-08-14", "last_synced_at": "2026-09-07T08:26:27.431Z", "location_count": 3, "location_summary": "New Brunswick, New Jersey • Newark, New Jersey", "locations": [ { "city": "New Brunswick", "state": "New Jersey" }, { "city": "New Brunswick", "state": "New Jersey" }, { "city": "Newark", "state": "New Jersey" } ], "official_url": "https://clinicaltrials.gov/study/NCT04920344" }, { "nct_id": "NCT07121595", "title": "Personalized Neck Radiation Therapy Directed by Sentinel Lymph Node Biopsy for the Treatment of Oral Cavity Squamous Cell Carcinoma, PRECEDENT Trial", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Oral Cavity Squamous Cell Carcinoma", "Stage I Lip and Oral Cavity Cancer AJCC v8", "Stage II Lip and Oral Cavity Cancer AJCC v8", "Stage III Lip and Oral Cavity Cancer AJCC v8", "Stage IVA Lip and Oral Cavity Cancer AJCC v8" ], "interventions": [ { "name": "Biospecimen Collection", "type": "PROCEDURE" }, { "name": "Carboplatin", "type": "DRUG" }, { "name": "Cisplatin", "type": "DRUG" }, { "name": "Computed Tomography", "type": "PROCEDURE" }, { "name": "Modified Barium Swallow", "type": "PROCEDURE" }, { "name": "Paclitaxel", "type": "DRUG" }, { "name": "Positron Emission Tomography", "type": "PROCEDURE" }, { "name": "Questionnaire Administration", "type": "OTHER" }, { "name": "Radiation Therapy", "type": "RADIATION" }, { "name": "Sentinel Lymph Node Biopsy", "type": "PROCEDURE" }, { "name": "Single Photon Emission Computed Tomography", "type": "PROCEDURE" }, { "name": "Technetium Tc 99m-labeled Tilmanocept", "type": "RADIATION" }, { "name": "Technetium Tc-99m Sulfur Colloid", "type": "OTHER" } ], "intervention_types": [ "PROCEDURE", "DRUG", "OTHER", "RADIATION" ], "sponsor": "University of Michigan Rogel Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 50, "start_date": "2025-07-17", "completion_date": "2030-07-01", "has_results": false, "last_update_posted_date": "2026-07-31", "last_synced_at": "2026-09-07T08:26:27.431Z", "location_count": 1, "location_summary": "Ann Arbor, Michigan", "locations": [ { "city": "Ann Arbor", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT07121595" } ] }