{
  "api_version": "1",
  "request": {
    "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Cardiac+Tamponade&page=2",
    "query": {
      "condition": "Cardiac Tamponade",
      "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=Cardiac+Tamponade&page=1&page_size=10"
  },
  "source": "remote",
  "last_synced_at": "2026-07-23T21:18:42.488Z",
  "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": "NCT06078735",
      "title": "Vascular Closure With a Device Compared to Manual Compression After Atrial Fibrillation Ablation: The LockeT II Study",
      "overall_status": "RECRUITING",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Atrial Fibrillation",
        "Hemostasis"
      ],
      "interventions": [
        {
          "name": "Vascular closure with LockeT device",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "DEVICE"
      ],
      "sponsor": "Kansas City Heart Rhythm Research Foundation",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "18 Years and older"
      },
      "enrollment_count": 110,
      "start_date": "2023-10-02",
      "completion_date": "2024-12",
      "has_results": false,
      "last_update_posted_date": "2024-10-29",
      "last_synced_at": "2026-07-23T21:18:42.488Z",
      "location_count": 6,
      "location_summary": "Overland Park, Kansas • Independence, Missouri • Kansas City, Missouri",
      "locations": [
        {
          "city": "Overland Park",
          "state": "Kansas"
        },
        {
          "city": "Overland Park",
          "state": "Kansas"
        },
        {
          "city": "Independence",
          "state": "Missouri"
        },
        {
          "city": "Independence",
          "state": "Missouri"
        },
        {
          "city": "Kansas City",
          "state": "Missouri"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT06078735"
    },
    {
      "nct_id": "NCT06350695",
      "title": "The ROle of Compression StocKings in Heart Failure Patients",
      "overall_status": "RECRUITING",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Heart Failure，Congestive",
        "Leg Edema",
        "Venous Insufficiency",
        "Venous Ulcers"
      ],
      "interventions": [
        {
          "name": "low grade compression stockings (10-15 mmHg)",
          "type": "DEVICE"
        },
        {
          "name": "high grade compression stockings (20-30 mmHg)",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "DEVICE"
      ],
      "sponsor": "University of Maryland, Baltimore",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "18 Years and older"
      },
      "enrollment_count": 50,
      "start_date": "2024-01-17",
      "completion_date": "2026-01-01",
      "has_results": false,
      "last_update_posted_date": "2024-10-02",
      "last_synced_at": "2026-07-23T21:18:42.488Z",
      "location_count": 1,
      "location_summary": "Dallas, Texas",
      "locations": [
        {
          "city": "Dallas",
          "state": "Texas"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT06350695"
    },
    {
      "nct_id": "NCT04095416",
      "title": "Compression Wraps as Adjuvant Therapy in Management of Acute Systolic Heart Failure",
      "overall_status": "TERMINATED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Heart Failure; With Decompensation"
      ],
      "interventions": [
        {
          "name": "ACE compression wrap",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "DEVICE"
      ],
      "sponsor": "Henry Ford Health System",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": "85 Years",
        "sex": "ALL",
        "summary": "18 Years to 85 Years"
      },
      "enrollment_count": 32,
      "start_date": "2019-08-15",
      "completion_date": "2021-01-21",
      "has_results": true,
      "last_update_posted_date": "2022-03-29",
      "last_synced_at": "2026-07-23T21:18:42.488Z",
      "location_count": 1,
      "location_summary": "Detroit, Michigan",
      "locations": [
        {
          "city": "Detroit",
          "state": "Michigan"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT04095416"
    },
    {
      "nct_id": "NCT01771484",
      "title": "High Sodium Diet and External Abdominal Compression in POTS",
      "overall_status": "TERMINATED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "PHASE1"
      ],
      "conditions": [
        "Postural Orthostatic Tachycardia Syndrome"
      ],
      "interventions": [
        {
          "name": "External automated abdominal binder",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "DEVICE"
      ],
      "sponsor": "Vanderbilt University",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": "60 Years",
        "sex": "ALL",
        "summary": "18 Years to 60 Years"
      },
      "enrollment_count": 13,
      "start_date": "2012-12",
      "completion_date": "2017-01",
      "has_results": false,
      "last_update_posted_date": "2017-01-18",
      "last_synced_at": "2026-07-23T21:18:42.488Z",
      "location_count": 1,
      "location_summary": "Nashville, Tennessee",
      "locations": [
        {
          "city": "Nashville",
          "state": "Tennessee"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT01771484"
    },
    {
      "nct_id": "NCT00120965",
      "title": "AutoPulse Assisted Prehospital International Resuscitation Trial (ASPIRE)",
      "overall_status": "TERMINATED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "PHASE3"
      ],
      "conditions": [
        "Cardiac Arrest"
      ],
      "interventions": [
        {
          "name": "AutoPulse",
          "type": "DEVICE"
        },
        {
          "name": "Manual CPR",
          "type": "OTHER"
        }
      ],
      "intervention_types": [
        "DEVICE",
        "OTHER"
      ],
      "sponsor": "University of Washington",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "18 Years and older"
      },
      "enrollment_count": 1837,
      "start_date": "2004-06",
      "completion_date": "2005-03",
      "has_results": false,
      "last_update_posted_date": "2011-01-27",
      "last_synced_at": "2026-07-23T21:18:42.488Z",
      "location_count": 1,
      "location_summary": "Seattle, Washington",
      "locations": [
        {
          "city": "Seattle",
          "state": "Washington"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT00120965"
    },
    {
      "nct_id": "NCT04573660",
      "title": "Abbott Vascular Medical Device Registry",
      "overall_status": "RECRUITING",
      "study_type": "OBSERVATIONAL",
      "phases": [],
      "conditions": [
        "Acute Myocardial Infarction",
        "Restenoses, Coronary",
        "Coronary Artery Lesions",
        "Venous Embolism",
        "Arterial Embolism"
      ],
      "interventions": [
        {
          "name": "Coronary and peripheral stents",
          "type": "DEVICE"
        },
        {
          "name": "Pacing catheters",
          "type": "DEVICE"
        },
        {
          "name": "Vascular plugs",
          "type": "DEVICE"
        },
        {
          "name": "Measurement and imaging (FFR and OCT)",
          "type": "DEVICE"
        },
        {
          "name": "Peripheral dilatation catheters",
          "type": "DEVICE"
        },
        {
          "name": "Coronary dilatation catheters",
          "type": "DEVICE"
        },
        {
          "name": "Coronary and peripheral guidewires",
          "type": "DEVICE"
        },
        {
          "name": "Vessel closure/compression devices",
          "type": "DEVICE"
        },
        {
          "name": "Vascular access introducers",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "DEVICE"
      ],
      "sponsor": "Abbott Medical Devices",
      "sponsor_class": "INDUSTRY",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "18 Years and older"
      },
      "enrollment_count": 3784,
      "start_date": "2020-10-25",
      "completion_date": "2031-11",
      "has_results": false,
      "last_update_posted_date": "2025-07-03",
      "last_synced_at": "2026-07-23T21:18:42.488Z",
      "location_count": 7,
      "location_summary": "Birmingham, Alabama • Little Rock, Arkansas • Los Angeles, California + 4 more",
      "locations": [
        {
          "city": "Birmingham",
          "state": "Alabama"
        },
        {
          "city": "Little Rock",
          "state": "Arkansas"
        },
        {
          "city": "Los Angeles",
          "state": "California"
        },
        {
          "city": "Chicago",
          "state": "Illinois"
        },
        {
          "city": "Lincoln",
          "state": "Nebraska"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT04573660"
    },
    {
      "nct_id": "NCT00842179",
      "title": "Groin Complications Post Percutaneous Coronary Intervention Using Either Manual Compression or PERCLOSE Device",
      "overall_status": "COMPLETED",
      "study_type": "OBSERVATIONAL",
      "phases": [],
      "conditions": [
        "Vascular Closure"
      ],
      "interventions": [],
      "intervention_types": [],
      "sponsor": "Clinyx, LLC",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "18 Years and older"
      },
      "enrollment_count": 2517,
      "start_date": "2008-06",
      "completion_date": "2008-10",
      "has_results": false,
      "last_update_posted_date": "2009-02-12",
      "last_synced_at": "2026-07-23T21:18:42.488Z",
      "location_count": 1,
      "location_summary": "Miami, Florida",
      "locations": [
        {
          "city": "Miami",
          "state": "Florida"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT00842179"
    },
    {
      "nct_id": "NCT04072484",
      "title": "Effectiveness of Chest Compressions Under Mild Hypoxia",
      "overall_status": "TERMINATED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Cardiac Arrest",
        "Hypoxia"
      ],
      "interventions": [
        {
          "name": "Mild hypoxia",
          "type": "OTHER"
        }
      ],
      "intervention_types": [
        "OTHER"
      ],
      "sponsor": "University of Chicago",
      "sponsor_class": "OTHER",
      "healthy_volunteers": true,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": "70 Years",
        "sex": "ALL",
        "summary": "18 Years to 70 Years"
      },
      "enrollment_count": 19,
      "start_date": "2019-08-16",
      "completion_date": "2020-10-01",
      "has_results": false,
      "last_update_posted_date": "2020-11-04",
      "last_synced_at": "2026-07-23T21:18:42.488Z",
      "location_count": 1,
      "location_summary": "Chicago, Illinois",
      "locations": [
        {
          "city": "Chicago",
          "state": "Illinois"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT04072484"
    },
    {
      "nct_id": "NCT06199414",
      "title": "Vascular Closure With Novel External Compression Device: The LockeT Study",
      "overall_status": "UNKNOWN",
      "study_type": "OBSERVATIONAL",
      "phases": [],
      "conditions": [
        "Atrial Fibrillation",
        "Hemostasis"
      ],
      "interventions": [
        {
          "name": "Venous Closure",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "DEVICE"
      ],
      "sponsor": "Kansas City Heart Rhythm Research Foundation",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "18 Years and older"
      },
      "enrollment_count": 70,
      "start_date": "2024-01",
      "completion_date": "2024-12",
      "has_results": false,
      "last_update_posted_date": "2024-01-10",
      "last_synced_at": "2026-07-23T21:18:42.488Z",
      "location_count": 2,
      "location_summary": "Overland Park, Kansas",
      "locations": [
        {
          "city": "Overland Park",
          "state": "Kansas"
        },
        {
          "city": "Overland Park",
          "state": "Kansas"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT06199414"
    },
    {
      "nct_id": "NCT05969028",
      "title": "First Responder Airway & Compression Rate Trial",
      "overall_status": "RECRUITING",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Out-Of-Hospital Cardiac Arrest"
      ],
      "interventions": [
        {
          "name": "igel",
          "type": "DEVICE"
        },
        {
          "name": "Compression Rate",
          "type": "PROCEDURE"
        }
      ],
      "intervention_types": [
        "DEVICE",
        "PROCEDURE"
      ],
      "sponsor": "University of Washington",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "18 Years and older"
      },
      "enrollment_count": 4200,
      "start_date": "2024-02-07",
      "completion_date": "2029-03",
      "has_results": false,
      "last_update_posted_date": "2024-06-13",
      "last_synced_at": "2026-07-23T21:18:42.488Z",
      "location_count": 1,
      "location_summary": "Seattle, Washington",
      "locations": [
        {
          "city": "Seattle",
          "state": "Washington"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT05969028"
    }
  ]
}