- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00501501
The Association Between Delivery Method and Maternal Rehospitalization
July 13, 2007 updated by: Western Galilee Hospital-Nahariya
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.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed 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.
Study Type
Observational
Enrollment (Actual)
92
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Nahariya, Israel, 22100
- Western Galilee Hospital
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 50 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- Parturients rehospitalized after delivery
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 1999
Study Completion (Actual)
December 1, 2000
Study Registration Dates
First Submitted
July 13, 2007
First Submitted That Met QC Criteria
July 13, 2007
First Posted (Estimate)
July 16, 2007
Study Record Updates
Last Update Posted (Estimate)
July 16, 2007
Last Update Submitted That Met QC Criteria
July 13, 2007
Last Verified
July 1, 2007
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 5
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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