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

Not Applicable

Completed

• Conditions: Postpartum Hemorrhage
• Interventions: Device: CAPP use

• Registration Number: NCT01497756
• Lead Sponsor: University of New Mexico

Brief 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.

Detailed Description

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

Study Timeline

• Study Start: 2011-08
• Study First Submitted: 2011-12-20
• Study First Submitted QC: 2011-12-21
• Study First Posted: 2011-12-22
• Primary Completion: 2012-05
• Study Completion: 2012-05
• Results First Submitted: 2012-07-02
• Results First Submitted QC: 2012-08-17
• Results First Posted: 2012-09-17
• Status Verified: 2020-02
• Last Update Submitted: 2020-02-25
• Last Update Posted: 2020-02-26

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 10

Inclusion Criteria

• Any patient receiving CAPP during study period.

Exclusion Criteria

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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
CAPP application	CAPP use	Patients in whom device is used

Primary Outcome Measures

Name	Time	Method
Usage	Eight months	Number of patients on whom CAPP is used

Secondary Outcome Measures

Name	Time	Method
Side Effects	Eight months	Any recorded complications

Trial Locations

Locations (1)

University of New Mexico; 🇺🇸 Albuquerque, New Mexico, United States