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Complications: Urgent C Section VS Elective C Section

This study is currently recruiting participants.
Verified December 2016 by Hadassah Medical Organization
Sponsor:
ClinicalTrials.gov Identifier:
NCT01524107
First Posted: February 1, 2012
Last Update Posted: December 20, 2016
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
Information provided by (Responsible Party):
Hadassah Medical Organization
  Purpose
The medical literature does not provide sufficient information or recommendation regarding specific antibiotic coverage for urgent Caesarian sections. The goal of this study is to compare maternal and neonatal morbidity of women who have undergone urgent Caesarian Sections for Prolapsed Cord to those who have undergone Elective Caesarian Sections in order to develop a standard treatment protocol. The Medical Record review will include many parameters including complications, type of antibiotic usage etc.

Condition
Urgent Caesarian Section Secondary to Cord Prolapse

Study Type: Observational
Study Design: Observational Model: Case Control
Time Perspective: Retrospective
Official Title: Comparison of Maternal and Fetal Complications After Urgent Caesarian Section for Prolapsed Cord Versus Elective Caesarian Section.

Resource links provided by NLM:


Further study details as provided by Hadassah Medical Organization:

Estimated Enrollment: 240
Study Start Date: January 2012
Estimated Primary Completion Date: December 2017 (Final data collection date for primary outcome measure)
Groups/Cohorts
Urgent Caesarian Section
Elective Caesarian Section

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   20 Years to 40 Years   (Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Women undergoing Urgent Caesarian Section for Prolapsed Cord and women undergoing Elective Caesarian Section at Hadassah Medical Center-Har HaTzofim.
Criteria

Inclusion Criteria:

  • women undergoing urgent Caesarian Section for Prolapsed Cord.
  • women undergoing Elective Caesarian Section.

Exclusion Criteria:

  • preterm birth
  • multiple gestation
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01524107


Contacts
Contact: Drorith Hochner-Celnikier, MD 00 972 2 5844400 hochner@hadassah.org.il

Locations
Israel
Hadassah Medical Organization Recruiting
Jerusalem, Israel
Contact: Hadas Lemberg, PhD    00 972 2 6777572    lhadas@hadassah.org.il   
Sponsors and Collaborators
Hadassah Medical Organization
Investigators
Principal Investigator: Drorith Hochner-Celnikier, MD Hadassah Medical Organization
  More Information

Responsible Party: Hadassah Medical Organization
ClinicalTrials.gov Identifier: NCT01524107     History of Changes
Other Study ID Numbers: CSURGENT-ELECT-HMO-CTIL
First Submitted: January 30, 2012
First Posted: February 1, 2012
Last Update Posted: December 20, 2016
Last Verified: December 2016

Keywords provided by Hadassah Medical Organization:
Prophylaxis Antibiotics
Maternal Complications
Neonatal Complications
Cord Prolapse
Elective Caesarian Section
Maternal Morbidity
Neonatal Morbidity

Additional relevant MeSH terms:
Prolapse
Pathological Conditions, Anatomical