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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 Oct 21, 2026, 7:28 AM 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 30, 2023 (Actual)
Primary completion
Dec 16, 2024 (Actual)
Completion
Jun 2025 (Estimated)
Last update posted
Jan 28, 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 28, 2025 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05653336 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →