{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Pharyngeal+Diseases&page=4", "query": { "condition": "Pharyngeal Diseases", "page": 4 }, "page_size": 10 }, "pagination": { "page": 4, "page_size": 10, "total_count": 709, "total_pages": 71, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Pharyngeal+Diseases&page=5&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Pharyngeal+Diseases&page=3&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-10T05:07:57.457Z", "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": "NCT04648020", "title": "Clonidine HCl MBT vs. Placebo to Prevent Chemoradiotherapy-Induced Severe Oral Mucositis in Oropharyngeal Cancer.", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2", "PHASE3" ], "conditions": [ "Chemoradiotherapy-Induced Severe Oral Mucositis" ], "interventions": [ { "name": "Clonidine HCl Mucoadhesive Buccal Tablet", "type": "DRUG" }, { "name": "Placebo Mucoadhesive Buccal Tablet", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Monopar Therapeutics", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 190, "start_date": "2021-02-11", "completion_date": "2023-05-14", "has_results": false, "last_update_posted_date": "2023-05-31", "last_synced_at": "2026-10-10T05:07:57.457Z", "location_count": 48, "location_summary": "Little Rock, Arkansas • Fountain Valley, California • Long Beach, California + 42 more", "locations": [ { "city": "Little Rock", "state": "Arkansas" }, { "city": "Fountain Valley", "state": "California" }, { "city": "Long Beach", "state": "California" }, { "city": "Pomona", "state": "California" }, { "city": "Grand Junction", "state": "Colorado" } ], "official_url": "https://clinicaltrials.gov/study/NCT04648020" }, { "nct_id": "NCT01199237", "title": "Impact of Anesthetic Choice (Sevoflurane Versus Desflurane) on Airway Reflex Recovery in the Context of Antagonized Neuromuscular Block", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Airway Reflexes, Protective", "Recovery After Neuromuscular Block", "Anesthetic Recovery" ], "interventions": [ { "name": "Sevoflurane", "type": "DRUG" }, { "name": "Desflurane", "type": "DRUG" }, { "name": "Rocuronium", "type": "DRUG" }, { "name": "Neostigmine", "type": "DRUG" }, { "name": "Glycopyrrolate", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "University of California, San Francisco", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "18 Years to 65 Years" }, "enrollment_count": 107, "start_date": "2010-08", "completion_date": "2013-08", "has_results": true, "last_update_posted_date": "2014-05-16", "last_synced_at": "2026-10-10T05:07:57.457Z", "location_count": 2, "location_summary": "San Francisco, California", "locations": [ { "city": "San Francisco", "state": "California" }, { "city": "San Francisco", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT01199237" }, { "nct_id": "NCT06583395", "title": "Quest to Analyze One Thousand Humans Meditating", "overall_status": "ENROLLING_BY_INVITATION", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Amyotrophic Lateral Sclerosis (ALS)", "Angina, Stable", "Anxiety", "Asthma", "Atrial Fibrillation", "Cancer Brain", "Cancer, Breast", "Cancer Colon", "Cancer, Lung", "Cancer, Ovarian", "Cancer Prostate", "Cancer Skin", "Throat Cancer", "Lymphoma", "Cancer, Thyroid", "Cancer, Other", "Cerebral Palsy", "Chronic Fatigue Syndrome", "Cluster Headache", "Chronic Obstructive Pulmonary Disease (COPD)", "Chronic Kidney Diseases", "Crohn Disease", "Deafness", "Depression", "Diabetes", "Eczema", "Epilepsy", "Fibroids", "Fibromyalgia", "Heart Failure", "Hypertension", "Hyperthyroidism", "Hypothyroidism", "Irritable Bowel Syndrome (IBS)", "Infertility", "Lyme Disease", "Macular Degeneration", "Migraine", "Multiple Allergies", "Multiple Sclerosis", "Osteoarthritis", "Osteoporosis", "Ovarian Cysts", "Parkinson Disease", "Phantom Limb Pain", "Psoriasis", "Post Traumatic Stress Disorder (PTSD)", "Rheumatoid Arthritis", "Sjogrens Disease", "Spinal Cord Injury", "Spinal Stenosis", "Stroke", "Tension Headache", "Tinnitus", "Ulcerative Colitis" ], "interventions": [ { "name": "Advanced multi-component meditation practice", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Tobias Moeller-Bertram", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "21 Years", "maximum_age": null, "sex": "ALL", "summary": "21 Years and older" }, "enrollment_count": 3000, "start_date": "2021-12-05", "completion_date": "2025-03-25", "has_results": false, "last_update_posted_date": "2024-11-01", "last_synced_at": "2026-10-10T05:07:57.457Z", "location_count": 1, "location_summary": "Palm Desert, California", "locations": [ { "city": "Palm Desert", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT06583395" }, { "nct_id": "NCT07780981", "title": "Impact of Body Positioning on EndoFLIP Measurements: A Comparative Study of Supine and Left Lateral Decubitus Positions", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Dysphagia", "Esophageal Stricture", "Epidermolysis Bullosa (EB)", "Achalasia", "Esophageal Motility Disorders", "Eosinophilic Esophagitis (EoE)" ], "interventions": [ { "name": "EndoFlip", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "DIAGNOSTIC_TEST" ], "sponsor": "Johns Hopkins University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "5 Years", "maximum_age": "21 Years", "sex": "ALL", "summary": "5 Years to 21 Years" }, "enrollment_count": 25, "start_date": "2026-07-24", "completion_date": "2028-07-01", "has_results": false, "last_update_posted_date": "2026-08-24", "last_synced_at": "2026-10-10T05:07:57.457Z", "location_count": 1, "location_summary": "Baltimore, Maryland", "locations": [ { "city": "Baltimore", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT07780981" }, { "nct_id": "NCT03387267", "title": "Videofluoroscopic Swallowing Study (VFSS)", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Stroke", "Parkinson Disease", "Multiple Sclerosis", "Oropharyngeal Dysphagia", "Alzheimer Disease", "Dementia" ], "interventions": [ { "name": "Dysphagia Detection System", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Société des Produits Nestlé (SPN)", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 452, "start_date": "2017-10-24", "completion_date": "2018-07-23", "has_results": true, "last_update_posted_date": "2025-12-19", "last_synced_at": "2026-10-10T05:07:57.457Z", "location_count": 12, "location_summary": "Downey, California • Aurora, Colorado • Washington D.C., District of Columbia + 8 more", "locations": [ { "city": "Downey", "state": "California" }, { "city": "Aurora", "state": "Colorado" }, { "city": "Washington D.C.", "state": "District of Columbia" }, { "city": "Chicago", "state": "Illinois" }, { "city": "Wheaton", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT03387267" }, { "nct_id": "NCT01721486", "title": "Acetaminophen's Efficacy For Post-operative Pain", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Tonsillitis", "Airway Obstruction", "Difficulty Swallowing" ], "interventions": [ { "name": "IV acetaminophen", "type": "DRUG" }, { "name": "PO acetaminophen", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Kaveh Aslani, MD", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "5 Years", "maximum_age": "13 Years", "sex": "ALL", "summary": "5 Years to 13 Years" }, "enrollment_count": 41, "start_date": "2012-09", "completion_date": "2015-01", "has_results": true, "last_update_posted_date": "2017-06-08", "last_synced_at": "2026-10-10T05:07:57.457Z", "location_count": 1, "location_summary": "Royal Oak, Michigan", "locations": [ { "city": "Royal Oak", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT01721486" }, { "nct_id": "NCT00498875", "title": "Depression and Adherence in Head and Neck Cancer", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Oropharyngeal Cancer", "Head and Neck Cancer" ], "interventions": [ { "name": "Questionnaire", "type": "BEHAVIORAL" }, { "name": "Depression Intervention", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "M.D. Anderson 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": 185, "start_date": "2005-03-15", "completion_date": "2026-12-31", "has_results": false, "last_update_posted_date": "2026-09-18", "last_synced_at": "2026-10-10T05:07:57.457Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT00498875" }, { "nct_id": "NCT06637774", "title": "The Aspirometer: A Noninvasive Tool for Detecting Aspiration Aim 3", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Deglutition Disorders" ], "interventions": [ { "name": "Aspirometer", "type": "DEVICE" }, { "name": "Videofluoroscopic X-ray", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of Pittsburgh", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "100 Years", "sex": "ALL", "summary": "18 Years to 100 Years" }, "enrollment_count": 50, "start_date": "2022-09-30", "completion_date": "2023-05-31", "has_results": true, "last_update_posted_date": "2025-02-19", "last_synced_at": "2026-10-10T05:07:57.457Z", "location_count": 1, "location_summary": "Pittsburgh, Pennsylvania", "locations": [ { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT06637774" }, { "nct_id": "NCT02045186", "title": "Monitoring of Oral Human Papillomavirus Infection (HPV) in HPV-positive Oropharyngeal Squamous Cell Carcinoma (OPSCC)", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Carcinoma, Squamous Cell", "Head and Neck Neoplasms", "Oropharyngeal Neoplasms" ], "interventions": [ { "name": "Assessment of Oral HPV Infection", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "UNC Lineberger Comprehensive Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "99 Years", "sex": "ALL", "summary": "18 Years to 99 Years" }, "enrollment_count": 1, "start_date": "2013-12", "completion_date": "2014-11", "has_results": false, "last_update_posted_date": "2017-05-04", "last_synced_at": "2026-10-10T05:07:57.457Z", "location_count": 1, "location_summary": "Chapel Hill, North Carolina", "locations": [ { "city": "Chapel Hill", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT02045186" }, { "nct_id": "NCT00004566", "title": "Study of Fetal Swallowing", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Deglutition Disorder", "High Risk Pregnancy" ], "interventions": [], "intervention_types": [], "sponsor": "National Institutes of Health Clinical Center (CC)", "sponsor_class": "NIH", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 120, "start_date": "2000-02", "completion_date": "2004-05", "has_results": false, "last_update_posted_date": "2008-03-04", "last_synced_at": "2026-10-10T05:07:57.457Z", "location_count": 1, "location_summary": "Bethesda, Maryland", "locations": [ { "city": "Bethesda", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT00004566" } ] }