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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00501501
Other study ID # 5
Secondary ID
Status Completed
Phase N/A
First received July 13, 2007
Last updated July 13, 2007
Start date January 1999
Est. completion date December 2000

Study information

Verified date July 2007
Source Western Galilee Hospital-Nahariya
Contact n/a
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Observational

Clinical Trial Summary

Hypothesis: The rates of rehospitalization after cesarean section are significantly higher than those following spontaneous vaginal delivery and are due mainly to late bleeding and less to infection.


Description:

To determine if there is an association between delivery method and maternal rehospitalization rate, the type of association and the reasons for rehospitalization.

The study population will consist women who were rehospitalized in the Western Galilee Hospital following cesarean section and after a vaginal delivery. Demographic data and hospitalization characteristics will be analyzed.


Recruitment information / eligibility

Status Completed
Enrollment 92
Est. completion date December 2000
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

- Parturients rehospitalized after delivery

Study Design

Observational Model: Defined Population, Time Perspective: Longitudinal


Related Conditions & MeSH terms


Intervention

Procedure:
Cesarean section

Vaginal delivery


Locations

Country Name City State
Israel Western Galilee Hospital Nahariya

Sponsors (1)

Lead Sponsor Collaborator
Western Galilee Hospital-Nahariya

Country where clinical trial is conducted

Israel, 

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