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Active, not recruiting Not applicable Interventional

PerQseal® Clinical Study

ClinicalTrials.gov ID: NCT05653336

Public ClinicalTrials.gov record NCT05653336. 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 Sep 4, 2026, 7:50 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

A Multicentre, Single-Arm, Pivotal Study to Evaluate the Safety and Efficacy of the Vivasure PerQseal® Closure Device System When Used to Achieve Haemostasis of Common Femoral Arteriotomies Created by 12 to 22 F Sheaths in Patients Undergoing Percutaneous Catheter-Based Interventional Procedures

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The objective is to evaluate the safety and effectiveness of the PerQseal vascular closure device system when used to achieve haemostasis of common femoral arteriotomies created by 12 to 22 F sheaths (arteriotomy up to 26 F) in subjects undergoing percutaneous catheter-based interventional procedures.

Study identification

NCT ID
NCT05653336
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Not applicable
Lead sponsor
Vivasure Medical Limited
Industry
Enrollment
149 participants

Conditions and interventions

Eligibility (public fields only)

Age range
19 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
Mar 29, 2023
Primary completion
Dec 15, 2024
Completion
May 31, 2025
Last update posted
Jan 27, 2025

2023 – 2025

United States locations

U.S. sites
15
U.S. states
8
U.S. cities
15
Facility City State ZIP Site status
HonorHealth Scottsdale Arizona 85258
Scripps La Jolla California 92037
Northern Light Eastern Maine Medical Center Bangor Maine 04401
Cooper University Hospital Camden New Jersey 08103
The Valley Hospital Paramus New Jersey 07652
University of Buffalo Buffalo New York 14203
Columbia University Medical Center/ NewYork Presbyterian Hospital New York New York 10032
University of Rochester Medical Center Rochester New York 14623
Stony Brook University Hospital Stony Brook New York 11794
Montefiore Medical Center (multiple centers) The Bronx New York 10461
The Cleveland Clinic Cleveland Ohio 44195
UPMC Pinnacle Health Mechanicsburg Pennsylvania 17050
UPenn - Perelman Center for Advanced Medicine, Philadelphia Pennsylvania 19104
Lankenau Institute for Medical Research Wynnewood Pennsylvania 19096
The Texas Heart Institute Houston Texas 77030

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 3 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05653336, 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 Jan 27, 2025 · Synced Sep 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05653336 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →