Feasibility Trial of the Circumferential Abdominal Pelvic Pressure Device (CAPP)

Completed · Not applicable

Conditions studied: Postpartum Hemorrhage

In brief

A group of midwives and obstetric nurses have been trained to use circumferential abdominal pelvic pressure (CAPP) to treat postpartum hemorrhage. As part of the training follow up any use of a CAPP device will be monitored to identify complications.

Key facts

Study ID

NCT01497756

Run by

University of New Mexico

People needed

10

Starts

2011-08-01

Expected to finish

2012-05-01

Last updated by the study team

2020-02-26

Who can join

Age: any. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Any patient receiving CAPP during study period.

You may not qualify if…

• None (CAPP is only clinically indicated for obstetric hemorrhage post delivery.

Where it is running

• University of New Mexico — Albuquerque, New Mexico, United States

Full record on ClinicalTrials.gov

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