{
  "api_version": "1",
  "request": {
    "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Medical+Device+Complication&page=2",
    "query": {
      "condition": "Medical Device Complication",
      "page": 2
    },
    "page_size": 10
  },
  "pagination": {
    "page": 2,
    "page_size": 10,
    "total_count": 10,
    "total_pages": 1,
    "next_page_url": null,
    "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Medical+Device+Complication&page=1&page_size=10"
  },
  "source": "remote",
  "last_synced_at": "2026-07-23T19:02:13.618Z",
  "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": "NCT05782296",
      "title": "Noninvasive Monitoring of Uterine Activity and Fetal Heart Rate",
      "overall_status": "COMPLETED",
      "study_type": "OBSERVATIONAL",
      "phases": [],
      "conditions": [
        "Fetal Heart Rate or Rhythm Abnormality Affecting Newborn During Labor",
        "Uterine Contractions",
        "Obstetric Complication"
      ],
      "interventions": [
        {
          "name": "TrueLabor",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "DEVICE"
      ],
      "sponsor": "OB-Tools Ltd.",
      "sponsor_class": "INDUSTRY",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "FEMALE",
        "summary": "18 Years and older · Female only"
      },
      "enrollment_count": 80,
      "start_date": "2022-02-24",
      "completion_date": "2024-06-05",
      "has_results": false,
      "last_update_posted_date": "2025-03-27",
      "last_synced_at": "2026-07-23T19:02:13.618Z",
      "location_count": 2,
      "location_summary": "Hoffman Estates, Illinois • The Bronx, New York",
      "locations": [
        {
          "city": "Hoffman Estates",
          "state": "Illinois"
        },
        {
          "city": "The Bronx",
          "state": "New York"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT05782296"
    },
    {
      "nct_id": "NCT06073145",
      "title": "Transcranial Doppler Using Wearable Ultrasound Patch",
      "overall_status": "COMPLETED",
      "study_type": "OBSERVATIONAL",
      "phases": [],
      "conditions": [
        "Medical Device Complication",
        "Brain Injuries",
        "Brain Diseases",
        "Stroke",
        "Vasospasm"
      ],
      "interventions": [
        {
          "name": "conventional transcranial Doppler probe and wearable ultrasound patch.",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "DEVICE"
      ],
      "sponsor": "University of California, San Diego",
      "sponsor_class": "OTHER",
      "healthy_volunteers": true,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "18 Years and older"
      },
      "enrollment_count": 36,
      "start_date": "2022-09-27",
      "completion_date": "2024-04-08",
      "has_results": false,
      "last_update_posted_date": "2024-04-10",
      "last_synced_at": "2026-07-23T19:02:13.618Z",
      "location_count": 1,
      "location_summary": "San Diego, California",
      "locations": [
        {
          "city": "San Diego",
          "state": "California"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT06073145"
    },
    {
      "nct_id": "NCT05445115",
      "title": "The Mollie Study, a Study to Evaluate the Safety and Efficacy of the Mollie Medical Device",
      "overall_status": "UNKNOWN",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Dyspareunia"
      ],
      "interventions": [
        {
          "name": "Mollie device",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "DEVICE"
      ],
      "sponsor": "JSP Innovations",
      "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": 111,
      "start_date": "2021-09-14",
      "completion_date": "2023-04-30",
      "has_results": false,
      "last_update_posted_date": "2022-07-06",
      "last_synced_at": "2026-07-23T19:02:13.618Z",
      "location_count": 1,
      "location_summary": "Decatur, Illinois",
      "locations": [
        {
          "city": "Decatur",
          "state": "Illinois"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT05445115"
    },
    {
      "nct_id": "NCT04469218",
      "title": "A Clinical Trial Using a New Medical Device to Evaluate Its Impact on IV Care and Clinical Complications",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "IV Catheter-Related Infection or Complication"
      ],
      "interventions": [
        {
          "name": "SafeBreak Vascular",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "DEVICE"
      ],
      "sponsor": "Lineus Medical",
      "sponsor_class": "INDUSTRY",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "18 Years and older"
      },
      "enrollment_count": 148,
      "start_date": "2020-07-14",
      "completion_date": "2020-12-31",
      "has_results": true,
      "last_update_posted_date": "2024-01-16",
      "last_synced_at": "2026-07-23T19:02:13.618Z",
      "location_count": 1,
      "location_summary": "Hartford, Connecticut",
      "locations": [
        {
          "city": "Hartford",
          "state": "Connecticut"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT04469218"
    },
    {
      "nct_id": "NCT03533400",
      "title": "Effectiveness of Jamboxx Respiratory Therapy Device: Study 1",
      "overall_status": "WITHDRAWN",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Spinal Cord Injuries",
        "Respiratory Complication"
      ],
      "interventions": [
        {
          "name": "Jamboxx Respiratory Therapy Device",
          "type": "DEVICE"
        },
        {
          "name": "Jamboxx Musical Device",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "DEVICE"
      ],
      "sponsor": "My Music Machines Inc.",
      "sponsor_class": "INDUSTRY",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "18 Years and older"
      },
      "enrollment_count": 0,
      "start_date": "2019-12-01",
      "completion_date": "2019-12-31",
      "has_results": false,
      "last_update_posted_date": "2020-05-13",
      "last_synced_at": "2026-07-23T19:02:13.618Z",
      "location_count": 1,
      "location_summary": "Albany, New York",
      "locations": [
        {
          "city": "Albany",
          "state": "New York"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT03533400"
    },
    {
      "nct_id": "NCT01937195",
      "title": "AccuCath™ Intravenous (IV) Device Used by Vascular Access Team (VAT)",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Vascular Access Complication"
      ],
      "interventions": [
        {
          "name": "AccuCath Intravenous Catheter System",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "DEVICE"
      ],
      "sponsor": "C. R. Bard",
      "sponsor_class": "INDUSTRY",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": "89 Years",
        "sex": "ALL",
        "summary": "18 Years to 89 Years"
      },
      "enrollment_count": 95,
      "start_date": "2013-04",
      "completion_date": "2014-11",
      "has_results": true,
      "last_update_posted_date": "2017-04-20",
      "last_synced_at": "2026-07-23T19:02:13.618Z",
      "location_count": 1,
      "location_summary": "Lewisburg, Pennsylvania",
      "locations": [
        {
          "city": "Lewisburg",
          "state": "Pennsylvania"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT01937195"
    },
    {
      "nct_id": "NCT05702242",
      "title": "A Randomized Controlled Trial of No Strings Intrauterine Device (IUD) Removal Techniques",
      "overall_status": "ACTIVE_NOT_RECRUITING",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "IUD Threads Not Visible",
        "IUD Removal Complication"
      ],
      "interventions": [
        {
          "name": "IUD removal with no visible strings",
          "type": "PROCEDURE"
        },
        {
          "name": "Alligator forceps",
          "type": "DEVICE"
        },
        {
          "name": "Manual Vacuum Aspirator",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "PROCEDURE",
        "DEVICE"
      ],
      "sponsor": "University of Colorado, Denver",
      "sponsor_class": "OTHER",
      "healthy_volunteers": true,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": "45 Years",
        "sex": "FEMALE",
        "summary": "18 Years to 45 Years · Female only"
      },
      "enrollment_count": 75,
      "start_date": "2023-01-01",
      "completion_date": "2024-12",
      "has_results": false,
      "last_update_posted_date": "2024-10-01",
      "last_synced_at": "2026-07-23T19:02:13.618Z",
      "location_count": 1,
      "location_summary": "Denver, Colorado",
      "locations": [
        {
          "city": "Denver",
          "state": "Colorado"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT05702242"
    },
    {
      "nct_id": "NCT04522778",
      "title": "Innovative Central Line Securement Device in the Pediatric Population",
      "overall_status": "TERMINATED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Central Line Complication",
        "Central Line Infection",
        "Central Line-Associated Infection",
        "Central Line Sepsis",
        "Short Gut Syndrome",
        "Quality of Life",
        "Pediatric Disorder"
      ],
      "interventions": [
        {
          "name": "Wearable Central Line Securement Device (Vest)",
          "type": "DEVICE"
        },
        {
          "name": "Traditional Securement Dressing",
          "type": "OTHER"
        }
      ],
      "intervention_types": [
        "DEVICE",
        "OTHER"
      ],
      "sponsor": "Ryan St. Pierre-Hetz",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "0 Years",
        "maximum_age": "18 Years",
        "sex": "ALL",
        "summary": "0 Years to 18 Years"
      },
      "enrollment_count": 23,
      "start_date": "2020-11-05",
      "completion_date": "2023-05-01",
      "has_results": true,
      "last_update_posted_date": "2024-07-05",
      "last_synced_at": "2026-07-23T19:02:13.618Z",
      "location_count": 1,
      "location_summary": "Pittsburgh, Pennsylvania",
      "locations": [
        {
          "city": "Pittsburgh",
          "state": "Pennsylvania"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT04522778"
    },
    {
      "nct_id": "NCT06358040",
      "title": "Opioid Dispenser for Microdiscectomy/Laminectomy",
      "overall_status": "RECRUITING",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Opioid Use",
        "Pain, Postoperative",
        "Medical Device",
        "Laminectomy",
        "Diskectomy"
      ],
      "interventions": [
        {
          "name": "Opioid-Dispensing Device",
          "type": "DEVICE"
        },
        {
          "name": "App",
          "type": "OTHER"
        },
        {
          "name": "Standard Opioid Pill Bottle",
          "type": "OTHER"
        }
      ],
      "intervention_types": [
        "DEVICE",
        "OTHER"
      ],
      "sponsor": "Hospital for Special Surgery, New York",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "18 Years and older"
      },
      "enrollment_count": 30,
      "start_date": "2026-10",
      "completion_date": "2026-12",
      "has_results": false,
      "last_update_posted_date": "2025-12-08",
      "last_synced_at": "2026-07-23T19:02:13.618Z",
      "location_count": 1,
      "location_summary": "New York, New York",
      "locations": [
        {
          "city": "New York",
          "state": "New York"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT06358040"
    },
    {
      "nct_id": "NCT00395447",
      "title": "REPLACE: Implantable Cardiac Pulse Generator Replacement Registry",
      "overall_status": "COMPLETED",
      "study_type": "OBSERVATIONAL",
      "phases": [],
      "conditions": [
        "Device Replacement",
        "Elective Replacement (ERI)",
        "Device Advisory",
        "Device Upgrade",
        "Postoperative Complications"
      ],
      "interventions": [
        {
          "name": "Straight-forward Device Replacement",
          "type": "PROCEDURE"
        },
        {
          "name": "Device Replacement with Upgrade",
          "type": "PROCEDURE"
        }
      ],
      "intervention_types": [
        "PROCEDURE"
      ],
      "sponsor": "Biotronik, Inc.",
      "sponsor_class": "INDUSTRY",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "18 Years and older"
      },
      "enrollment_count": 1744,
      "start_date": "2007-07",
      "completion_date": "2009-06",
      "has_results": true,
      "last_update_posted_date": "2015-04-14",
      "last_synced_at": "2026-07-23T19:02:13.618Z",
      "location_count": 71,
      "location_summary": "Birmingham, Alabama • Mesa, Arizona • Modesto, California + 58 more",
      "locations": [
        {
          "city": "Birmingham",
          "state": "Alabama"
        },
        {
          "city": "Mesa",
          "state": "Arizona"
        },
        {
          "city": "Modesto",
          "state": "California"
        },
        {
          "city": "Rancho Mirage",
          "state": "California"
        },
        {
          "city": "Sacramento",
          "state": "California"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT00395447"
    }
  ]
}