{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=INFECTIONS&page=15", "query": { "condition": "INFECTIONS", "page": 15 }, "page_size": 10 }, "pagination": { "page": 15, "page_size": 10, "total_count": 259, "total_pages": 26, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=INFECTIONS&page=16&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=INFECTIONS&page=14&page_size=10" }, "source": "local", "last_synced_at": "2026-10-17T04:21:53.645Z", "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": "NCT07864636", "title": "Automatic Versus As-Needed Follow-up After Hospitalization for Children With Medical Complexity", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Acute Gastroenteritis", "Children With Medical Complexity", "Respiratory Tract Infections (RTI)", "Skin and Soft Tissue Infection", "Urinary Tract Infection (UTI)" ], "interventions": [ { "name": "As-needed follow-up recommendation", "type": "BEHAVIORAL" }, { "name": "Automatic follow-up recommendation", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Seattle Children's Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "1 Year", "maximum_age": "16 Years", "sex": "ALL", "summary": "1 Year to 16 Years" }, "enrollment_count": 160, "start_date": "2026-10", "completion_date": "2028-09", "has_results": false, "last_update_posted_date": "2026-10-08", "last_synced_at": "2026-10-14T00:13:42.539Z", "location_count": 1, "location_summary": "Seattle, Washington", "locations": [ { "city": "Seattle", "state": "Washington" } ], "official_url": "https://clinicaltrials.gov/study/NCT07864636" }, { "nct_id": "NCT07462767", "title": "Precision Microbiota Interventions for Senoreduction Trial", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1", "PHASE2" ], "conditions": [ "Aging", "Alcohol Drinking", "HIV Infections", "Immunosenescence" ], "interventions": [ { "name": "Blueberry extract", "type": "DIETARY_SUPPLEMENT" }, { "name": "Limosilactobacillus reuteri", "type": "DIETARY_SUPPLEMENT" } ], "intervention_types": [ "DIETARY_SUPPLEMENT" ], "sponsor": "Louisiana State University Health Sciences Center in New Orleans", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "40 Years", "maximum_age": null, "sex": "ALL", "summary": "40 Years and older" }, "enrollment_count": 160, "start_date": "2026-10-01", "completion_date": "2029-12-01", "has_results": false, "last_update_posted_date": "2026-10-01", "last_synced_at": "2026-10-13T20:36:05.758Z", "location_count": 1, "location_summary": "New Orleans, Louisiana", "locations": [ { "city": "New Orleans", "state": "Louisiana" } ], "official_url": "https://clinicaltrials.gov/study/NCT07462767" }, { "nct_id": "NCT07371429", "title": "A Study in Pediatric Participants Aged ≥2 to <12 Years With a Suspected or Confirmed Bacterial Infection or Receiving Prophylaxis Antibiotics", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Urinary Tract Infections" ], "interventions": [ { "name": "Gepotidacin", "type": "DRUG" }, { "name": "SOC", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "GlaxoSmithKline", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "2 Years", "maximum_age": "11 Years", "sex": "ALL", "summary": "2 Years to 11 Years" }, "enrollment_count": 25, "start_date": "2026-09-18", "completion_date": "2027-08-23", "has_results": false, "last_update_posted_date": "2026-09-28", "last_synced_at": "2026-10-16T22:49:57.452Z", "location_count": 4, "location_summary": "Orange, California • Shreveport, Louisiana • Baltimore, Maryland + 1 more", "locations": [ { "city": "Orange", "state": "California" }, { "city": "Shreveport", "state": "Louisiana" }, { "city": "Baltimore", "state": "Maryland" }, { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT07371429" }, { "nct_id": "NCT07535346", "title": "Integrating Supports to Promote PrEP for Black Adolescents Working With Apps- Atlanta", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "HIV Infections" ], "interventions": [ { "name": "Health MPowerment App", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Emory University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "14 Years", "maximum_age": "21 Years", "sex": "ALL", "summary": "14 Years to 21 Years" }, "enrollment_count": 10, "start_date": "2027-04", "completion_date": "2027-04", "has_results": false, "last_update_posted_date": "2026-09-22", "last_synced_at": "2026-10-16T20:11:56.114Z", "location_count": 1, "location_summary": "Atlanta, Georgia", "locations": [ { "city": "Atlanta", "state": "Georgia" } ], "official_url": "https://clinicaltrials.gov/study/NCT07535346" }, { "nct_id": "NCT07828691", "title": "18F-FDG PET/CT for Diagnosis of Diabetic Foot Osteomyelitis", "overall_status": "NOT_YET_RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Diabetic Foot Infections" ], "interventions": [ { "name": "18F-FDG PET/CT", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "DIAGNOSTIC_TEST" ], "sponsor": "Jewish General Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 150, "start_date": "2026-11", "completion_date": "2029-04", "has_results": false, "last_update_posted_date": "2026-09-18", "last_synced_at": "2026-10-16T19:43:41.115Z", "location_count": 1, "location_summary": "Dallas, Texas", "locations": [ { "city": "Dallas", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT07828691" }, { "nct_id": "NCT07792915", "title": "A Clinical Trial of Resistant Potato Starch for Gut MDRO Decolonization", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Asymptomatic Infections", "Carbapenem-Resistant Enterobacteriaceae", "Clostridium Infections", "Methicillin-resistant Staphylococcus Aureus (MRSA)", "Vancomycin-Resistant Enterococci" ], "interventions": [ { "name": "Maltodextrin", "type": "DRUG" }, { "name": "Resistant Potato Starch", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "VA Office of Research and Development", "sponsor_class": "FED", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 120, "start_date": "2027-01-01", "completion_date": "2030-09-30", "has_results": false, "last_update_posted_date": "2026-08-28", "last_synced_at": "2026-08-30T02:28:45.189Z", "location_count": 1, "location_summary": "Madison, Wisconsin", "locations": [ { "city": "Madison", "state": "Wisconsin" } ], "official_url": "https://clinicaltrials.gov/study/NCT07792915" }, { "nct_id": "NCT06854029", "title": "NOTRE: Optimizing Long-Acting Pre-Exposure Prophylaxis and Medications for Opioid Use Disorder Interventions in Carceral Settings", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "HIV Infections", "Incarceration; Lens", "Opioid Use Disorder" ], "interventions": [ { "name": "Buprenorphine Pill", "type": "DRUG" }, { "name": "Buprenorphine injection", "type": "DRUG" }, { "name": "Cabotegravir Injection", "type": "DRUG" }, { "name": "Cabotegravir Pill", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Duke University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 450, "start_date": "2026-09-01", "completion_date": "2030-06-01", "has_results": false, "last_update_posted_date": "2026-08-26", "last_synced_at": "2026-10-17T04:21:53.645Z", "location_count": 1, "location_summary": "Durham, North Carolina", "locations": [ { "city": "Durham", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT06854029" }, { "nct_id": "NCT07322289", "title": "Antibiotic-coated Braided Suture Study", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Debridement With Prosthesis Retention", "Prosthetic Joint Infection", "Prosthetic Joint Infections of Hip", "Prosthetic Joint Infections of Knee", "Suture" ], "interventions": [ { "name": "Polydioxanone (PDS™ II ) Sterile Synthetic Absorbable Surgical Suture-Monofilament", "type": "DEVICE" }, { "name": "VICRYL™ Plus (Coated VICRYL™ Plus Antibacterial)", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of Miami", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "89 Years", "sex": "ALL", "summary": "18 Years to 89 Years" }, "enrollment_count": 142, "start_date": "2026-11-01", "completion_date": "2027-12-31", "has_results": false, "last_update_posted_date": "2026-07-08", "last_synced_at": "2026-08-09T10:02:19.636Z", "location_count": 1, "location_summary": "Miami, Florida", "locations": [ { "city": "Miami", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT07322289" }, { "nct_id": "NCT06068283", "title": "An mHealth Intervention to Improve HIV Prevention Service Engagement Among People Who Use Drugs", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "HIV Infections" ], "interventions": [ { "name": "LOTUS mHealth Intervention Group", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of California, San Diego", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 40, "start_date": "2026-07-01", "completion_date": "2027-07-30", "has_results": false, "last_update_posted_date": "2026-06-26", "last_synced_at": "2026-08-02T05:03:56.394Z", "location_count": 1, "location_summary": "La Jolla, California", "locations": [ { "city": "La Jolla", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT06068283" }, { "nct_id": "NCT07525076", "title": "Implementation of an Opt-Out Testing and Rapid Diagnostic Strategy for Syphilis and HIV in Pregnant Patients Presenting to the Emergency Department", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "HIV Infections", "Syphilis Infection" ], "interventions": [ { "name": "Chembio HIV/Syphilis rapid Point of Care (POC) test", "type": "DIAGNOSTIC_TEST" }, { "name": "Laboratory-based HIV and syphilis testing", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "DIAGNOSTIC_TEST" ], "sponsor": "The University of Texas Health Science Center, Houston", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "14 Years", "maximum_age": "45 Years", "sex": "FEMALE", "summary": "14 Years to 45 Years · Female only" }, "enrollment_count": 1400, "start_date": "2026-04-15", "completion_date": "2028-05-31", "has_results": false, "last_update_posted_date": "2026-04-13", "last_synced_at": "2026-10-14T02:26:39.340Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT07525076" } ] }