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

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.

Completed

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Key information

Conditions

Postpartum Hemorrhage Female Urogenital Diseases and Pregnancy Complications Hemorrhage Obstetric Labor Complications Pathologic Processes Pathological Conditions, Signs and Symptoms Pregnancy Complications Puerperal Disorders Urogenital Diseases Uterine Hemorrhage

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

University of New Mexico

Albuquerque, New Mexico, 81435, United States

About this study

Providers will be surveyed twice at 4 and 8 months using open ended methods.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Any patient receiving CAPP during study period.

Exclusion criteria

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

Treatment and study plan

CAPP use

Device

Any abdominal pelvic pressure

Primary outcomes

Usage

Time frame: Eight months

Number of patients on whom CAPP is used

Secondary outcomes

Side Effects

Time frame: Eight months

Any recorded complications

Sponsors and collaborators

Lead sponsor

University of New Mexico

Other

Registry information

Important dates

Study start: 2011
Primary completion: 2012
Study completion: 2012
First posted: Dec 22, 2011
Registry last updated: Feb 26, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed