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NCT01497756 Clinical Trial

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

Postpartum Hemorrhage Clinical Trial

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

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01497756
Other study ID # 10-229
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 2011
Est. completion date May 2012

Study information
Verified date February 2020
Source University of New Mexico
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.

Description:

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

Recruitment information / eligibility
Status Completed
Enrollment 10
Est. completion date May 2012
Est. primary completion date May 2012
Accepts healthy volunteers No
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria:

- Any patient receiving CAPP during study period.

Exclusion Criteria:

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

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• CAPP use
Any abdominal pelvic pressure

Locations
Country Name City State
United States University of New Mexico Albuquerque New Mexico

Sponsors (1)
Lead Sponsor Collaborator
University of New Mexico

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Usage Number of patients on whom CAPP is used Eight months
Secondary Side Effects Any recorded complications Eight months
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