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Efficacy Study of the Non-Pneumatic Anti-Shock Garment (NASG) in Egypt

NCT00305253 · Status: COMPLETED · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL · Enrollment: 990

Last updated 2013-05-14

Study results available
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Summary

This study will test the efficacy of the NASG on women suffering from obstetric hemorrhage as compared to hemorrhaging women who do not receive the NASG.

Conditions

Interventions

DEVICE

Non-pneumatic Anti-shock Garment (NASG)

In the Post-Intrevention phase of the study, the NASG will be used when a patient meets the study criteria.

Sponsors & Collaborators

Principal Investigators

  • Suellen Miller, CNM, PhD, RN · University of California, San Francisco

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-04-30
Primary Completion
2008-06-30
Completion
2008-06-30

Countries

  • Egypt

Study Locations

More Related Trials

Entities

Diseases
Companies

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 NCT00305253 on ClinicalTrials.gov