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NCT03052699 Clinical Trial

Medium and Long-term Complications of the Patients Having Had a Vaginal Caesarian in Hospital René Dubos

Complications; Cesarean Section Clinical Trial

— CeVag  

Official title:
Medium and Long-term Complications of the Patients Having Had a Vaginal Caesarian in Hospital René Dubos

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03052699
Other study ID # CHRD1115
Secondary ID
Status Completed
Phase N/A
First received September 13, 2016
Last updated February 10, 2017
Start date September 2015
Est. completion date November 2015

Study information
Verified date February 2017
Source Centre Hospitalier René Dubos
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This database has for objective to include the medical data of patients which underwent a vaginal Cesarean Section in our establishment. This collection will allow to determine the risk factors of the maternal morbi-mortality and to estimate the long-term results

Description:

It is about an operating technique little known which is used as an alternative of the abdominal Cesarean Section for very premature pregnancies and the main indication is the maternal rescue.

It has several advantages: simplicity of the technique, the dissection of tissues is limited, low risk of bleeding and no abdominal scar.

The purpose is to determine the risk factors of the maternal morbi-mortality and to estimate the long-term results

Recruitment information / eligibility
Status Completed
Enrollment 26
Est. completion date November 2015
Est. primary completion date November 2015
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- patients operated to vaginal Cesarean in Hospital Rene DUBOS

Exclusion Criteria:

- patients followed in a maternity which do not participate to the study

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• vaginal Cesarean Section
follow-up to patients operated for vaginal Cesarean Section

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Centre Hospitalier René Dubos

Outcome
Type Measure Description Time frame Safety issue
Primary Risk factors of the maternal morbi-mortality by collection of adverse events during the pregnancy, concomitant pathologies and antecedents 1 day
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