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Completed Not applicable Interventional Results available

Cross-Seal Closure Device IDE Trial - Study of the Cross-SealTM Suture-Mediated Vascular Closure Device System

ClinicalTrials.gov ID: NCT03756558

Public ClinicalTrials.gov record NCT03756558. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 12:19 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Cross-SealTM IDE Trial: Prospective, Multi-Center, Single Arm Study of the Cross-SealTM Suture-Mediated Vascular Closure Device System

Study identification

NCT ID
NCT03756558
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Terumo Medical Corporation
Industry
Enrollment
147 participants

Conditions and interventions

Interventions

  • Cross-Seal System Device

Device

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 8, 2019
Primary completion
Mar 21, 2021
Completion
Mar 21, 2021
Last update posted
Sep 14, 2025

2019 – 2021

United States locations

U.S. sites
20
U.S. states
14
U.S. cities
18
Facility City State ZIP Site status
Vascular Institute of the Rockies Denver Colorado 80218
River City Clinical Research Jacksonville Florida 32207
University of South Florida Tampa Florida 33620
University of Iowa Hospital Iowa City Iowa 52242
Beth Israel Deaconess Medical Center Boston Massachusetts 02215
Rutgers, The State University of New Jersey Piscataway New Jersey 08854
Mt Sinai Medical Center New York New York 10029
The Trustees of Columbia University in the City of New York New York New York 10032
University of Rochester Rochester New York 14642
Good Samaritan Hospital Cincinnati Ohio 45220
Cleveland Clinic Cleveland Ohio 44195
INTEGRIS Cardiovascular Physicians Oklahoma City Oklahoma 73112
Lankenau Institute for Medical Research Wynnewood Pennsylvania 19096
North Central Heart Sioux Falls South Dakota 57108
Holston Valley Medical Center Kingsport Tennessee 37660
Cardiothoracic and Vascular Surgeons Austin Texas 78756
St. David's Heart and Vascular dba Austin heart Austin Texas 78756
Texas Heart Institute and Baylor St. Luke's Medical Center Houston Texas 77030
Sentara Medical Group Norfolk Virginia 23502
Swedish Medical Center Seattle Washington 98122

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03756558, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 14, 2025 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03756558 live on ClinicalTrials.gov.

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