{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=kanamycin", "query": { "intervention": "kanamycin" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 42, "total_pages": 5, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=kanamycin&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-09-07T07:26:44.274Z", "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": "NCT00198523", "title": "A Bioequivalence Study of Tobramycin and Prednisolone Acetate Compared to PredForte", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Eye Infections", "Postoperative Complications" ], "interventions": [ { "name": "Prednisolone and Tobramycin", "type": "DRUG" }, { "name": "Prednisolone", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Bausch & Lomb Incorporated", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 132, "start_date": "2005-07", "completion_date": "2005-10", "has_results": false, "last_update_posted_date": "2013-03-15", "last_synced_at": "2026-09-07T07:26:44.274Z", "location_count": 6, "location_summary": "Great Bend, Kansas • Boston, Massachusetts • Saint Joseph, Michigan + 3 more", "locations": [ { "city": "Great Bend", "state": "Kansas" }, { "city": "Boston", "state": "Massachusetts" }, { "city": "Saint Joseph", "state": "Michigan" }, { "city": "Portsmouth", "state": "New Hampshire" }, { "city": "Austin", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT00198523" }, { "nct_id": "NCT01431326", "title": "Pharmacokinetics of Understudied Drugs Administered to Children Per Standard of Care", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Adenovirus", "Anesthesia", "Anxiety", "Anxiolysis", "Autism", "Autistic Disorder", "Bacterial Meningitis", "Bacterial Septicemia", "Benzodiazepine", "Bipolar Disorder", "Bone and Joint Infections", "Central Nervous System Infections", "Convulsions", "Cytomegalovirus Retinitis", "Early-onset Schizophrenia Spectrum Disorders", "Epilepsy", "General Anesthesia", "Gynecologic Infections", "Herpes Simplex Virus", "Infantile Hemangioma", "Infection", "Inflammation", "Inflammatory Conditions", "Intra-abdominal Infections", "Lower Respiratory Tract Infections", "Migraines", "Pain", "Pneumonia", "Schizophrenia", "Sedation", "Seizures", "Skeletal Muscle Spasms", "Skin and Skin-structure Infections", "Treatment-resistant Schizophrenia", "Urinary Tract Infections", "Withdrawal", "Sepsis", "Gram-negative Infection", "Bradycardia", "Cardiac Arrest", "Cardiac Arrhythmia", "Staphylococcal Infections", "Nosocomial Pneumonia", "Neuromuscular Blockade", "Methicillin Resistant Staphylococcus Aureus", "Endocarditis", "Neutropenia", "Headache", "Fibrinolytic Bleeding", "Pulmonary Arterial Hypertension", "CMV Retinitis", "Hypertension", "Chronic Kidney Diseases", "Hyperaldosteronism", "Hypokalemia", "Heart Failure", "Hemophilia", "Heavy Menstrual Bleeding", "Insomnia" ], "interventions": [ { "name": "The POPS study is collecting PK data on children prescribed the following drugs of interest per standard of care:", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Daniel Benjamin", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": "21 Years", "sex": "ALL", "summary": "Up to 21 Years" }, "enrollment_count": 3520, "start_date": "2011-11", "completion_date": "2019-11", "has_results": false, "last_update_posted_date": "2023-09-06", "last_synced_at": "2026-09-07T07:26:44.274Z", "location_count": 43, "location_summary": "Anchorage, Alaska • Little Rock, Arkansas • La Jolla, California + 37 more", "locations": [ { "city": "Anchorage", "state": "Alaska" }, { "city": "Little Rock", "state": "Arkansas" }, { "city": "La Jolla", "state": "California" }, { "city": "Los Angeles", "state": "California" }, { "city": "Los Angeles", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT01431326" }, { "nct_id": "NCT04964947", "title": "Tobramycin Injection to Prevent Infection in Open Fractures", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Wound Infection", "Fractures, Open", "Surgical Site Infection" ], "interventions": [ { "name": "Tobramycin Injection", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Massachusetts General Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "18 Years to 80 Years" }, "enrollment_count": 600, "start_date": "2022-01-10", "completion_date": "2026-07", "has_results": false, "last_update_posted_date": "2026-05-15", "last_synced_at": "2026-09-07T07:26:44.274Z", "location_count": 3, "location_summary": "Lexington, Kentucky • Boston, Massachusetts • Nashville, Tennessee", "locations": [ { "city": "Lexington", "state": "Kentucky" }, { "city": "Boston", "state": "Massachusetts" }, { "city": "Nashville", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT04964947" }, { "nct_id": "NCT01659866", "title": "Antibiotic Prophylaxis for Transrectal Prostate Biopsy", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Infection" ], "interventions": [ { "name": "Ciprofloxacin", "type": "DRUG" }, { "name": "trimethoprim-sulfamethoxazole", "type": "DRUG" }, { "name": "cefuroxime", "type": "DRUG" }, { "name": "ceftriaxone", "type": "DRUG" }, { "name": "gentamicin", "type": "DRUG" }, { "name": "amikacin", "type": "DRUG" }, { "name": "aztreonam", "type": "DRUG" }, { "name": "imipenem", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Northwestern University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "30 Years", "maximum_age": "90 Years", "sex": "MALE", "summary": "30 Years to 90 Years · Male only" }, "enrollment_count": 563, "start_date": "2012-08", "completion_date": "2016-08", "has_results": true, "last_update_posted_date": "2019-06-25", "last_synced_at": "2026-09-07T07:26:44.274Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT01659866" }, { "nct_id": "NCT05429671", "title": "Antibiotic Loaded Cement After TKA", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Total Knee Arthoplasty" ], "interventions": [ { "name": "total knee arthroplasty", "type": "PROCEDURE" }, { "name": "Tobramycin", "type": "DRUG" }, { "name": "Gentamicin", "type": "DRUG" }, { "name": "Antibiotic cement spacer", "type": "DEVICE" } ], "intervention_types": [ "PROCEDURE", "DRUG", "DEVICE" ], "sponsor": "Rothman Institute Orthopaedics", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 50, "start_date": "2022-06-20", "completion_date": "2023-11-30", "has_results": false, "last_update_posted_date": "2024-04-30", "last_synced_at": "2026-09-07T07:26:44.274Z", "location_count": 1, "location_summary": "Philadelphia, Pennsylvania", "locations": [ { "city": "Philadelphia", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT05429671" }, { "nct_id": "NCT02478710", "title": "Aerosolized Antibiotics in the Treatment of Ventilator Associated Pneumonia", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Pneumonia, Ventilator-Associated" ], "interventions": [ { "name": "Aerosolized Tobramycin or Vancomycin", "type": "DRUG" }, { "name": "Aerosolized Placebo", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Wright State University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 16, "start_date": "2015-06", "completion_date": "2022-07", "has_results": true, "last_update_posted_date": "2023-05-31", "last_synced_at": "2026-09-07T07:26:44.274Z", "location_count": 1, "location_summary": "Dayton, Ohio", "locations": [ { "city": "Dayton", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT02478710" }, { "nct_id": "NCT01456780", "title": "Efficacy of Zylet vs. Lotemax for the Treatment of Ocular Surface Inflammation/MGD/Blepharitis", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Meibomian Gland Dysfunction", "Posterior Blepharitis" ], "interventions": [ { "name": "Loteprednol/tobramycin", "type": "DRUG" }, { "name": "Loteprednol", "type": "DRUG" }, { "name": "B+L Advanced Eye Relief Lubricant Drop", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Massachusetts Eye and Ear Infirmary", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 60, "start_date": "2011-08", "completion_date": "2017-06", "has_results": true, "last_update_posted_date": "2017-08-01", "last_synced_at": "2026-09-07T07:26:44.274Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT01456780" }, { "nct_id": "NCT05227937", "title": "Single Dose Amikacin for Uncomplicated Cystitis in the ED: A Feasibility Study", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Urinary Tract Infections" ], "interventions": [ { "name": "Amikacin", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Antonios Likourezos", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "14 Years", "maximum_age": "110 Years", "sex": "FEMALE", "summary": "14 Years to 110 Years · Female only" }, "enrollment_count": 75, "start_date": "2022-09-21", "completion_date": "2026-12-31", "has_results": false, "last_update_posted_date": "2026-03-04", "last_synced_at": "2026-09-07T07:26:44.274Z", "location_count": 1, "location_summary": "Brooklyn, New York", "locations": [ { "city": "Brooklyn", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT05227937" }, { "nct_id": "NCT02099240", "title": "Patients Response to Early Switch To Oral:Osteomyelitis Study", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "EARLY_PHASE1" ], "conditions": [ "Osteomyelitis" ], "interventions": [ { "name": "oral antibiotics", "type": "DRUG" }, { "name": "intravenous antibiotics", "type": "PROCEDURE" } ], "intervention_types": [ "DRUG", "PROCEDURE" ], "sponsor": "Julio Ramirez", "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": 11, "start_date": "2014-03-06", "completion_date": "2018-11-07", "has_results": false, "last_update_posted_date": "2021-04-06", "last_synced_at": "2026-09-07T07:26:44.274Z", "location_count": 1, "location_summary": "Louisville, Kentucky", "locations": [ { "city": "Louisville", "state": "Kentucky" } ], "official_url": "https://clinicaltrials.gov/study/NCT02099240" }, { "nct_id": "NCT00153634", "title": "Standard vs. Biofilm Susceptibility Testing in Cystic Fibrosis (CF)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Cystic Fibrosis", "Chronic Bronchitis" ], "interventions": [ { "name": "IV amikacin", "type": "DRUG" }, { "name": "PO azithromycin", "type": "DRUG" }, { "name": "IV ceftazidime", "type": "DRUG" }, { "name": "PO ciprofloxacin", "type": "DRUG" }, { "name": "IV meropenem", "type": "DRUG" }, { "name": "IV piperacillin-tazobactam", "type": "DRUG" }, { "name": "IV ticarcillin-clavulanate", "type": "DRUG" }, { "name": "IV tobramycin", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Seattle Children's Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "14 Years", "maximum_age": null, "sex": "ALL", "summary": "14 Years and older" }, "enrollment_count": 75, "start_date": "2004-03", "completion_date": "2007-11", "has_results": false, "last_update_posted_date": "2008-03-13", "last_synced_at": "2026-09-07T07:26:44.274Z", "location_count": 8, "location_summary": "Iowa City, Iowa • St Louis, Missouri • Cincinnati, Ohio + 4 more", "locations": [ { "city": "Iowa City", "state": "Iowa" }, { "city": "St Louis", "state": "Missouri" }, { "city": "Cincinnati", "state": "Ohio" }, { "city": "Columbus", "state": "Ohio" }, { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT00153634" } ] }