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

NCT01497756 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 10

Last updated 2020-02-26

Study results available
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Summary

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.

Conditions

  • Postpartum Hemorrhage

Interventions

DEVICE

CAPP use

Any abdominal pelvic pressure

Sponsors & Collaborators

  • University of New Mexico

    lead OTHER

Principal Investigators

  • Mark Hauswald, MD · University of New Mexico

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-08-31
Primary Completion
2012-05-31
Completion
2012-05-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01497756 on ClinicalTrials.gov