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Completed Not applicable Interventional Results available

MANTA Percutaneous Vascular Closure Device - The SAFE MANTA Study

ClinicalTrials.gov ID: NCT02908880

Public ClinicalTrials.gov record NCT02908880. 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 20, 2026, 8:53 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

Pivotal Clinical Study to EvaluAte the SaFety and Effectiveness of MANTA Vascular Closure Device

Brief summary

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

Research study which tests the safety and effectiveness of a new vascular closure device to close the femoral access puncture that is created in patients who require this form of access in order to perform the planned procedure. The MANTA device is expected to seal the femoral access puncture in less than 1 minute. This may result in less blood loss and a shorter time to walking compared to alternative closure means. Use of the MANTA device in this study is experimental. All other parts of the procedure involve standard medical care.

Study identification

NCT ID
NCT02908880
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Essential Medical, Inc.
Industry
Enrollment
263 participants

Conditions and interventions

Eligibility (public fields only)

Age range
21 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
Dec 2016 (Type not available)
Primary completion
Oct 2017 (Actual)
Completion
Dec 2017 (Actual)
Last update posted
Sep 25, 2019

2016 – 2017

United States locations

U.S. sites
18
U.S. states
14
U.S. cities
17
Facility City State ZIP Site status
San Diego VA Medical Center San Diego California 92161 —
Washington Hospital Center Washington D.C. District of Columbia 20010 —
Evanston Hospital Evanston Illinois 60201 —
St. Vincent Heart Center Indianapolis Indiana 46290 —
Henry Ford Detroit Michigan 48202 —
St. Luke Hospital (Mid America Heart) Kansas City Missouri 64111 —
Columbia University Medical Center New York New York 10032 —
Cleveland Clinic Cleveland Ohio 44195 —
Hershey Medical Center Hershey Pennsylvania 17033 —
Temple University Hospital Philadelphia Pennsylvania 19140 —
Lankenau Heart Group Wynnewood Pennsylvania 19096 —
Avera Heart Hospital Sioux Falls South Dakota 57108 —
Wellmont Holston Valley Hospital Kingsport Tennessee 37660 —
Houston Methodist Houston Texas 77030 —
St. Luke's Hospital - Texas Heart Houston Texas 77030 —
The Heart Hospital Baylor Plano Plano Texas 75093 —
Swedish Medical Center Seattle Washington 98122 —
CAMC Memorial Hospital Charleston West Virginia 25304 —

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 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02908880, 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 25, 2019 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02908880 live on ClinicalTrials.gov.

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