{
  "api_version": "1",
  "request": {
    "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Folliculitis",
    "query": {
      "condition": "Folliculitis"
    },
    "page_size": 10
  },
  "pagination": {
    "page": 1,
    "page_size": 10,
    "total_count": 13,
    "total_pages": 2,
    "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Folliculitis&page=2&page_size=10",
    "previous_page_url": null
  },
  "source": "remote",
  "last_synced_at": "2026-06-26T20:12:47.212Z",
  "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": "NCT01126268",
      "title": "Twice Daily Altabax Application for the Treatment of Uncomplicated Soft Tissue Infection",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "PHASE4"
      ],
      "conditions": [
        "Impetigo",
        "Folliculitis",
        "Secondarily Infected Eczema",
        "Minor Soft Tissue Infections"
      ],
      "interventions": [
        {
          "name": "Retapamulin (Altabax)",
          "type": "DRUG"
        }
      ],
      "intervention_types": [
        "DRUG"
      ],
      "sponsor": "The University of Texas Health Science Center, Houston",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "9 Months",
        "maximum_age": "98 Years",
        "sex": "ALL",
        "summary": "9 Months to 98 Years"
      },
      "enrollment_count": 38,
      "start_date": "2010-04",
      "completion_date": "2012-11",
      "has_results": true,
      "last_update_posted_date": "2016-02-17",
      "last_synced_at": "2026-06-26T20:12:47.212Z",
      "location_count": 1,
      "location_summary": "Houston, Texas",
      "locations": [
        {
          "city": "Houston",
          "state": "Texas"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT01126268"
    },
    {
      "nct_id": "NCT04214483",
      "title": "A Pilot Study to Explore the Role of Gut Flora in Acne",
      "overall_status": "WITHDRAWN",
      "study_type": "OBSERVATIONAL",
      "phases": [],
      "conditions": [
        "Acne",
        "Acne Vulgaris",
        "Acne Keloidalis",
        "Acne Keloid",
        "Acne Conglobata",
        "Acne Rosacea",
        "Acne Inversa",
        "Acne Cystic",
        "Acne Pomade",
        "Acne Indurata",
        "Acne Papular",
        "Acne Tropica",
        "Acne Urticata",
        "Acne Fulminans",
        "Acne Follicular",
        "Acne Tropicalis",
        "Acne Detergicans",
        "Acne Iodide",
        "Acne Varioliformis"
      ],
      "interventions": [
        {
          "name": "No intervention",
          "type": "OTHER"
        }
      ],
      "intervention_types": [
        "OTHER"
      ],
      "sponsor": "ProgenaBiome",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": null,
        "maximum_age": null,
        "sex": "ALL",
        "summary": "Not listed"
      },
      "enrollment_count": 0,
      "start_date": "2020-03-02",
      "completion_date": "2030-07",
      "has_results": false,
      "last_update_posted_date": "2025-06-05",
      "last_synced_at": "2026-06-26T20:12:47.212Z",
      "location_count": 1,
      "location_summary": "Ventura, California",
      "locations": [
        {
          "city": "Ventura",
          "state": "California"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT04214483"
    },
    {
      "nct_id": "NCT00746109",
      "title": "Study of Wound Packing After Superficial Skin Abscess Drainage",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "PHASE4"
      ],
      "conditions": [
        "Abscess",
        "Skin Diseases, Infectious",
        "Boils",
        "Furuncle",
        "Carbuncle",
        "Folliculitis",
        "Cellulitis",
        "Wounds"
      ],
      "interventions": [
        {
          "name": "Wound packing",
          "type": "PROCEDURE"
        },
        {
          "name": "NoPacking",
          "type": "PROCEDURE"
        }
      ],
      "intervention_types": [
        "PROCEDURE"
      ],
      "sponsor": "NYU Langone Health",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "1 Year",
        "maximum_age": "24 Years",
        "sex": "ALL",
        "summary": "1 Year to 24 Years"
      },
      "enrollment_count": 60,
      "start_date": "2008-09",
      "completion_date": "2010-03",
      "has_results": false,
      "last_update_posted_date": "2011-01-04",
      "last_synced_at": "2026-06-26T20:12:47.212Z",
      "location_count": 1,
      "location_summary": "New York, New York",
      "locations": [
        {
          "city": "New York",
          "state": "New York"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT00746109"
    },
    {
      "nct_id": "NCT01328080",
      "title": "Treatment of Acne Keloidalis Nuchae (Razor Bumps Behind the Neck) Using UV Light Therapy",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Acne Keloidalis Nuchae"
      ],
      "interventions": [
        {
          "name": "Targeted UV-B",
          "type": "RADIATION"
        }
      ],
      "intervention_types": [
        "RADIATION"
      ],
      "sponsor": "Johns Hopkins University",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "MALE",
        "summary": "18 Years and older · Male only"
      },
      "enrollment_count": 11,
      "start_date": "2011-02",
      "completion_date": "2012-08",
      "has_results": true,
      "last_update_posted_date": "2017-03-29",
      "last_synced_at": "2026-06-26T20:12:47.212Z",
      "location_count": 1,
      "location_summary": "Baltimore, Maryland",
      "locations": [
        {
          "city": "Baltimore",
          "state": "Maryland"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT01328080"
    },
    {
      "nct_id": "NCT04807205",
      "title": "Post Market Study Using The Elite IQ Device",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Hair Removal",
        "Pseudo Folliculitis Barbae",
        "Benign Vascular Lesion",
        "Pigmented Lesions"
      ],
      "interventions": [
        {
          "name": "RF Non-Invasive Treatment",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "DEVICE"
      ],
      "sponsor": "Cynosure, Inc.",
      "sponsor_class": "INDUSTRY",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "18 Years and older"
      },
      "enrollment_count": 20,
      "start_date": "2021-03-26",
      "completion_date": "2022-03-02",
      "has_results": true,
      "last_update_posted_date": "2024-06-12",
      "last_synced_at": "2026-06-26T20:12:47.212Z",
      "location_count": 1,
      "location_summary": "San Diego, California",
      "locations": [
        {
          "city": "San Diego",
          "state": "California"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT04807205"
    },
    {
      "nct_id": "NCT00824863",
      "title": "Safety and Efficacy of Ketoconazole 2% Foam in the Treatment of Pityrosporum Folliculitis",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "PHASE4"
      ],
      "conditions": [
        "Pityrosporum Folliculitis"
      ],
      "interventions": [
        {
          "name": "ketoconazole 2% foam",
          "type": "DRUG"
        }
      ],
      "intervention_types": [
        "DRUG"
      ],
      "sponsor": "Wayne Fujita, M.D.",
      "sponsor_class": "INDIV",
      "healthy_volunteers": true,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": "65 Years",
        "sex": "ALL",
        "summary": "18 Years to 65 Years"
      },
      "enrollment_count": 10,
      "start_date": "2008-12",
      "completion_date": "2010-06",
      "has_results": false,
      "last_update_posted_date": "2014-08-21",
      "last_synced_at": "2026-06-26T20:12:47.212Z",
      "location_count": 1,
      "location_summary": "‘Aiea, Hawaii",
      "locations": [
        {
          "city": "‘Aiea",
          "state": "Hawaii"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT00824863"
    },
    {
      "nct_id": "NCT00129428",
      "title": "Ultraviolet B (UVB) Light Therapy in the Treatment of Skin Conditions With Altered Dermal Matrix",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "PHASE1",
        "PHASE2"
      ],
      "conditions": [
        "Keloid",
        "Scleroderma, Localized",
        "Acne Keloidalis",
        "Scars",
        "Granuloma Annulare"
      ],
      "interventions": [
        {
          "name": "UVB Irradiation",
          "type": "PROCEDURE"
        }
      ],
      "intervention_types": [
        "PROCEDURE"
      ],
      "sponsor": "University of Michigan",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "10 Years",
        "maximum_age": "80 Years",
        "sex": "ALL",
        "summary": "10 Years to 80 Years"
      },
      "enrollment_count": 33,
      "start_date": "2002-08",
      "completion_date": "2009-01",
      "has_results": false,
      "last_update_posted_date": "2015-05-01",
      "last_synced_at": "2026-06-26T20:12:47.212Z",
      "location_count": 1,
      "location_summary": "Ann Arbor, Michigan",
      "locations": [
        {
          "city": "Ann Arbor",
          "state": "Michigan"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT00129428"
    },
    {
      "nct_id": "NCT00289588",
      "title": "An Attempt to Reduce Community-Acquired Methicillin-Resistant Staphylococcus Aureus (MRSA) Infection in Soldiers",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Community-Acquired MRSA Infections",
        "Abscesses",
        "Cellulitis",
        "Folliculitis"
      ],
      "interventions": [
        {
          "name": "Mupirocin (drug)",
          "type": "DRUG"
        }
      ],
      "intervention_types": [
        "DRUG"
      ],
      "sponsor": "Brooke Army Medical Center",
      "sponsor_class": "FED",
      "healthy_volunteers": true,
      "eligibility": {
        "minimum_age": "17 Years",
        "maximum_age": "60 Years",
        "sex": "ALL",
        "summary": "17 Years to 60 Years"
      },
      "enrollment_count": 3000,
      "start_date": "2005-01",
      "completion_date": "2005-12",
      "has_results": false,
      "last_update_posted_date": "2006-02-16",
      "last_synced_at": "2026-06-26T20:12:47.212Z",
      "location_count": 1,
      "location_summary": "Fort Sam Houston, Texas",
      "locations": [
        {
          "city": "Fort Sam Houston",
          "state": "Texas"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT00289588"
    },
    {
      "nct_id": "NCT00757315",
      "title": "NdYag Laser for Acne Keloidalis Nuchae",
      "overall_status": "UNKNOWN",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Acne Keloidalis Nuchae",
        "NdYag Laser",
        "AKN",
        "Acne Keloidalis",
        "AK",
        "Dermatitis Papillaris Capillitii",
        "Folliculitis Keloidalis Nuchae",
        "Sycosis Nuchae",
        "Acne Keloid",
        "Keloidal Folliculitis",
        "Lichen Keloidalis Nuchae",
        "Folliculitis Nuchae Scleroticans",
        "Sycosis Framboesiformis"
      ],
      "interventions": [
        {
          "name": "NdYag Laser(hair removal laser) plus topical corticosteroid",
          "type": "DEVICE"
        },
        {
          "name": "Topical corticosteroid alone",
          "type": "DRUG"
        }
      ],
      "intervention_types": [
        "DEVICE",
        "DRUG"
      ],
      "sponsor": "Henry Ford Health System",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "18 Years and older"
      },
      "enrollment_count": 20,
      "start_date": "2008-09",
      "completion_date": "2013-12",
      "has_results": false,
      "last_update_posted_date": "2013-03-29",
      "last_synced_at": "2026-06-26T20:12:47.212Z",
      "location_count": 1,
      "location_summary": "Detroit, Michigan",
      "locations": [
        {
          "city": "Detroit",
          "state": "Michigan"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT00757315"
    },
    {
      "nct_id": "NCT05608499",
      "title": "Duobrii Treatment of Acne Keloidalis Nuchae (AKN)",
      "overall_status": "TERMINATED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "PHASE3"
      ],
      "conditions": [
        "Acne Keloidalis Nuchae",
        "AKN"
      ],
      "interventions": [
        {
          "name": "Duobrii",
          "type": "DRUG"
        },
        {
          "name": "Placebo",
          "type": "DRUG"
        },
        {
          "name": "Bryhali",
          "type": "DRUG"
        }
      ],
      "intervention_types": [
        "DRUG"
      ],
      "sponsor": "Icahn School of Medicine at Mount Sinai",
      "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": "2022-10-26",
      "completion_date": "2024-04-15",
      "has_results": true,
      "last_update_posted_date": "2025-11-04",
      "last_synced_at": "2026-06-26T20:12:47.212Z",
      "location_count": 1,
      "location_summary": "New York, New York",
      "locations": [
        {
          "city": "New York",
          "state": "New York"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT05608499"
    }
  ]
}