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Completed Not applicable Interventional Results available

HEMOBLAST Pivotal Clinical Investigation

ClinicalTrials.gov ID: NCT02780869

Public ClinicalTrials.gov record NCT02780869. 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 22, 2026, 5:36 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

Prospective, Randomized, Controlled, Multicenter, Pivotal, Clinical Investigation Evaluating the Safety and Efficacy of HEMOBLAST Bellows in Cardiothoracic, Abdominal, and Orthopedic Lower Extremity Surgeries

Brief summary

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

The purpose of this prospective, randomized, controlled study is to evaluate the safety and efficacy of a new hemostatic device (HEMOBLAST™ Bellows) compared to a control device, absorbable gelatin sponge USP with thrombin.

Study identification

NCT ID
NCT02780869
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Biom'Up France SAS
Industry
Enrollment
258 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
Jul 18, 2016 (Actual)
Primary completion
Feb 1, 2017 (Actual)
Completion
Mar 27, 2017 (Actual)
Last update posted
Dec 27, 2018

2016 – 2017

United States locations

U.S. sites
17
U.S. states
11
U.S. cities
15
Facility City State ZIP Site status
CORE Institute Phoenix Arizona — —
University of California Los Angeles Los Angeles California — —
University of Southern California Los Angeles California — —
Lotus Clinical Research Pasadena California — —
Miami Plastic Surgery Miami Florida — —
Queens Medical Center Honolulu Hawaii — —
Suburban Hospital - Johns Hopkins Medicine Bethesda Maryland 20814 —
Washington University in St. Louis St Louis Missouri — —
Dartmouth Hitchcock Medical Center Hanover New Hampshire — —
Columbia University Medical Center / New York Presbyterian Hospital New York New York — —
Icahn School of Medicine at Mount Sinai New York New York — —
University of North Carolina at Chapel Hill Chapel Hill North Carolina — —
Duke University Durham North Carolina — —
Hunstad Kortesis Center Huntsville North Carolina — —
Intermountain Liver Disease and Transplant Center Murray Utah — —
University of Virginia Charlottesville Virginia — —
Spectrum Medical Danville Virginia — —

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 NCT02780869, 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 Dec 27, 2018 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02780869 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →