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NCT02878226 Clinical Trial

Outcomes of Uterine Rupture

Maternal Mortality Clinical Trial

Official title:
Uterine Rupture: Prevalence and Feto-maternal Outcomes in Assiut Women Health Hospital

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02878226
Other study ID # UR
Secondary ID
Status Completed
Phase
First received
Last updated
Start date August 2016
Est. completion date February 18, 2018

Study information
Verified date June 2018
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Uterine rupture (UR) is a serious, life-threatening obstetric complication. UR is associated with an increased risk of maternal and perinatal morbidity and mortality, particularly in developing countries compared to developed countries. UR occurs mainly as a consequence of poorly managed labour

Recruitment information / eligibility
Status Completed
Enrollment 65
Est. completion date February 18, 2018
Est. primary completion date December 15, 2017
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria:

- women with ruptured uterus

- accept to share in the study

Exclusion Criteria:

- women refuse to participate

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• repair of rupture

Locations
Country Name City State
Egypt Ahmed Abbas Assiut Cairo

Sponsors (1)
Lead Sponsor Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary number of women undergoes repair 1 hour
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