{
  "api_version": "1",
  "request": {
    "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Nasal+Fracture",
    "query": {
      "condition": "Nasal Fracture"
    },
    "page_size": 10
  },
  "pagination": {
    "page": 1,
    "page_size": 10,
    "total_count": 4,
    "total_pages": 1,
    "next_page_url": null,
    "previous_page_url": null
  },
  "source": "remote",
  "last_synced_at": "2026-05-22T04:51:24.055Z",
  "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": "NCT06850857",
      "title": "Multi-Institutional IMPACT Validation",
      "overall_status": "ENROLLING_BY_INVITATION",
      "study_type": "OBSERVATIONAL",
      "phases": [],
      "conditions": [
        "Facial Injuries",
        "Mandible Fracture",
        "Le Fort",
        "Zygomaticomaxillary Complex Fracture",
        "Nasal Fracture",
        "Orbital Fractures",
        "Zygoma Fracture",
        "Orbital Floor Fracture",
        "Facial Laceration"
      ],
      "interventions": [
        {
          "name": "IMPACT-G Module",
          "type": "OTHER"
        },
        {
          "name": "IMPACT-N Module",
          "type": "OTHER"
        },
        {
          "name": "IMPACT-O Module",
          "type": "OTHER"
        },
        {
          "name": "IMPACT-J Module",
          "type": "OTHER"
        },
        {
          "name": "15D Control Survey",
          "type": "OTHER"
        }
      ],
      "intervention_types": [
        "OTHER"
      ],
      "sponsor": "University of Tennessee",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "18 Years and older"
      },
      "enrollment_count": 500,
      "start_date": "2025-07-01",
      "completion_date": "2026-12-31",
      "has_results": false,
      "last_update_posted_date": "2025-06-18",
      "last_synced_at": "2026-05-22T04:51:24.055Z",
      "location_count": 3,
      "location_summary": "Sacramento, California • San Francisco, California • Memphis, Tennessee",
      "locations": [
        {
          "city": "Sacramento",
          "state": "California"
        },
        {
          "city": "San Francisco",
          "state": "California"
        },
        {
          "city": "Memphis",
          "state": "Tennessee"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT06850857"
    },
    {
      "nct_id": "NCT03624608",
      "title": "Evaluation of the Auryzon Devices in the Optimization of Ear and Nose Reconstruction Procedures",
      "overall_status": "TERMINATED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Ear Deformities, Acquired",
        "Ear; Deformity, Congenital",
        "Microtia",
        "Nose Deformity",
        "Nose Deformities, Acquired",
        "Nose; Deformity, Congenital",
        "Nose; Deformity, Congenital, Bent or Squashed",
        "Nose; Deformity, Syphilitic, Congenital",
        "Nose; Deformity, Bone (Nose Cartilage)",
        "Nose; Deformity, Septum, Congenital",
        "Nose; Deformity, Sinus (Wall), Congenital",
        "Nose; Deformity, Syphilitic, Late (Etiology)",
        "Ear; Deformity, External",
        "Ear; Deformity, Auricle, Ear, Acquired",
        "Ear; Deformity, Auricle, Ear (Congenital)"
      ],
      "interventions": [
        {
          "name": "AuryzoN Family of Devices",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "DEVICE"
      ],
      "sponsor": "Reconstrata, LLC",
      "sponsor_class": "INDUSTRY",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": null,
        "maximum_age": null,
        "sex": "ALL",
        "summary": "Not listed"
      },
      "enrollment_count": 2,
      "start_date": "2020-03-01",
      "completion_date": "2025-01-20",
      "has_results": false,
      "last_update_posted_date": "2025-01-23",
      "last_synced_at": "2026-05-22T04:51:24.055Z",
      "location_count": 1,
      "location_summary": "Cincinnati, Ohio",
      "locations": [
        {
          "city": "Cincinnati",
          "state": "Ohio"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT03624608"
    },
    {
      "nct_id": "NCT05763602",
      "title": "PVI to Prevent S. Aureus SSI After Fixation of HELEF (POTENT Study)",
      "overall_status": "ACTIVE_NOT_RECRUITING",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "PHASE4"
      ],
      "conditions": [
        "Surgical Site Infection"
      ],
      "interventions": [
        {
          "name": "povidone-iodine topical ointment",
          "type": "DRUG"
        }
      ],
      "intervention_types": [
        "DRUG"
      ],
      "sponsor": "Loreen Herwaldt",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "18 Years and older"
      },
      "enrollment_count": 2000,
      "start_date": "2022-09-15",
      "completion_date": "2026-05-31",
      "has_results": false,
      "last_update_posted_date": "2026-02-04",
      "last_synced_at": "2026-05-22T04:51:24.055Z",
      "location_count": 6,
      "location_summary": "Atlanta, Georgia • Indianapolis, Indiana • Iowa City, Iowa + 3 more",
      "locations": [
        {
          "city": "Atlanta",
          "state": "Georgia"
        },
        {
          "city": "Indianapolis",
          "state": "Indiana"
        },
        {
          "city": "Iowa City",
          "state": "Iowa"
        },
        {
          "city": "St Louis",
          "state": "Missouri"
        },
        {
          "city": "Dallas",
          "state": "Texas"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT05763602"
    },
    {
      "nct_id": "NCT03780478",
      "title": "Preoperative Nerve Block for Rhinoplasty/Septoplasty",
      "overall_status": "UNKNOWN",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "PHASE1",
        "PHASE2"
      ],
      "conditions": [
        "Nasal Fracture",
        "Deviated Nasal Septum"
      ],
      "interventions": [
        {
          "name": "Nerve block",
          "type": "DRUG"
        },
        {
          "name": "Placebo Saline Injection",
          "type": "DRUG"
        }
      ],
      "intervention_types": [
        "DRUG"
      ],
      "sponsor": "University of Southern California",
      "sponsor_class": "OTHER",
      "healthy_volunteers": true,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "18 Years and older"
      },
      "enrollment_count": 70,
      "start_date": "2019-06-17",
      "completion_date": "2022-03-01",
      "has_results": false,
      "last_update_posted_date": "2019-07-30",
      "last_synced_at": "2026-05-22T04:51:24.055Z",
      "location_count": 1,
      "location_summary": "Los Angeles, California",
      "locations": [
        {
          "city": "Los Angeles",
          "state": "California"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT03780478"
    }
  ]
}