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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:
Hadassah Medical Organization
Information provided by (Responsible Party):
Hadassah Medical Organization
ClinicalTrials.gov Identifier:
NCT01524107
First received: January 30, 2012
Last updated: December 18, 2016
Last verified: December 2016
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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| 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
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study.
To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below.
For general information, see Learn About Clinical Studies.
Please refer to this study by its ClinicalTrials.gov identifier: NCT01524107
Please refer to this study by its ClinicalTrials.gov identifier: 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 |
| Study First Received: | January 30, 2012 |
| Last Updated: | December 18, 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 |
ClinicalTrials.gov processed this record on September 18, 2017