Postcesarean Section Pain: Possible Demographic and Medical Predictors

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified July 2006 by Rambam Health Care Campus.
Recruitment status was:  Not yet recruiting
Sponsor:
Information provided by:
Rambam Health Care Campus
ClinicalTrials.gov Identifier:
NCT00416104
First received: December 26, 2006
Last updated: NA
Last verified: July 2006
History: No changes posted
  Purpose
The aim of this retrospective study is to find out if one or more of the following parameters has an impact on postcesarean section pain:age,ethnic origin, parity,body habitus, smoking, breastfeeding, education,newborn in intensive care unit, primary/repeated operation,elective/emergency operation,junior/senior surgeon,type of anesthesia during operation.

Condition
Pain
Cesarean Section

Study Type: Observational
Study Design: Observational Model: Defined Population
Time Perspective: Cross-Sectional
Time Perspective: Retrospective
Official Title: Postcesarean Section Pain: Possible Demographic and Medical Predictors

Further study details as provided by Rambam Health Care Campus:

Estimated Enrollment: 600
Study Start Date: December 2006
Estimated Study Completion Date: February 2007
Detailed Description:
The medical records of 600 consecutive women with a cesarean section will be reviewed.We will analyse the correlations between postcesarean section pain levels,analgesic consumption and; age,ethnic origin, parity,body habitus, smoking, breastfeeding, education,newborn in intensive care unit, primary/repeated operation,elective/emergency operation,junior/senior surgeon,type of anesthesia during operation.
  Eligibility

Ages Eligible for Study:   Child, Adult, Senior
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Women undergoing a cesarean section

Exclusion Criteria:

  • Medical or psychological conditions not enabling reliable patients pain assessment
  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: NCT00416104

Locations
Israel
Rambam Medical Center
Haifa, Israel, 31096
Sponsors and Collaborators
Rambam Health Care Campus
Investigators
Principal Investigator: etan z zimmer, MD director of obstetrics rambam medical center
  More Information

ClinicalTrials.gov Identifier: NCT00416104     History of Changes
Other Study ID Numbers: zimmerctil 
Study First Received: December 26, 2006
Last Updated: December 26, 2006

Keywords provided by Rambam Health Care Campus:
analgesia

ClinicalTrials.gov processed this record on January 19, 2017