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

University of New Mexico (UNM)

Status: Completed

Conditions: Postpartum Hemorrhage

Treatments: Device: CAPP use

Study type: Interventional

Funder types: Other

Identifiers

NCT01497756

10-229

Details and patient eligibility

About

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.

Full description

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

Enrollment: 10 patients

Sex: Female

Volunteers: No Healthy Volunteers

Inclusion criteria

• Any patient receiving CAPP during study period.

Exclusion criteria

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

Trial design

Primary purpose: Other

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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10 participants in 1 patient group

CAPP application

Experimental group

Description:

Patients in whom device is used

Treatment:

Device: CAPP use