Last updated on September 2018

Safety and Effectiveness of the InPress Device in Treating Primary Postpartum Hemorrhage

Brief description of study

The purpose of this study is to evaluate the safety and effectiveness of the InPress Device in the control and reduction of primary postpartum hemorrhage.

Detailed Study Description

This IDE study is designed to evaluate the effectiveness and safety of the InPress Device to treat primary PPH. The study is literature controlled.

Clinical Study Identifier: NCT02883673

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Christina Duzyj, MD

Rutgers Robert Wood Johnson Medical
New Brunswick, NJ United States
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Dan Skupski, MD

New York Presbyterian Queens
Flushing, NY United States
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Dena Goffman, MD

Columbia University
New York, NY United States
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Kathryn D Wine, MPH

University of Texas Medical Branch
Galveston, TX United States
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Marcela Smid, MD

University of Utah
Salt Lake City, UT United States
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Jennifer Krupp, MD

St. Mary's Hospital
Madison, WI United States
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