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Completed Not applicable Interventional Results available

Progel Vascular Sealant

ClinicalTrials.gov ID: NCT01959503

Public ClinicalTrials.gov record NCT01959503. 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 23, 2026, 8:40 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 Prospective, Randomized Study to Compare Progel Vascular Sealant to Gelfoam Plus as an Adjunct for the Control of Bleeding in Subjects Undergoing Thoracic Aortic Surgery

Brief summary

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

This study is being conducted to evaluate the safety and effectiveness of the Progel Vascular Sealant for use in vascular reconstructions to achieve adjunctive hemostasis by mechanically sealing areas of leakage.

Study identification

NCT ID
NCT01959503
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
C. R. Bard
Industry
Enrollment
158 participants

Conditions and interventions

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
Nov 2013 (Type not available)
Primary completion
Dec 2014 (Actual)
Completion
Dec 2014 (Actual)
Last update posted
Apr 10, 2017

2013 – 2014

United States locations

U.S. sites
19
U.S. states
16
U.S. cities
19
Facility City State ZIP Site status
Cedars-Sinai Los Angeles California 90048 —
University of Colorado Aurora Colorado 80045 —
University of Florida Gainesville Florida 32610 —
Portneuf Hospital Pocatello Idaho 83201 —
Northwestern University Chicago Illinois 60611 —
University of Michigan Ann Arbor Michigan 48109 —
Mayo Clinic Hospital Rochester Minnesota 55905 —
Washington University St Louis Missouri 63110 —
Bryan Heart Lincoln Nebraska 68510 —
Cornell University New York New York 10021 —
Montefiore Medical Center The Bronx New York 10467 —
Carolinas Health Care System Charlotte North Carolina 28203 —
Ohio Health Research Institute Columbus Ohio 43214 —
University of Pennsylvania Philadelphia Pennsylvania 19104 —
Houston Methodist Hospital Houston Texas 77030 —
The Heart Hospital Baylor Plano Texas 75093 —
Intermountain Medical Center Murray Utah 84107 —
University of Virginia Health Sciences Center Charlottesville Virginia 22904 —
Virginia Commonwealth University Medical Center Richmond Virginia 23298 —

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 NCT01959503, 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 Apr 10, 2017 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01959503 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →