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Postcesarean Section Pain: Possible Demographic and Medical Predictors

The recruitment status of this study is unknown because the information has not been verified recently.
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

Resource links provided by NLM:

MedlinePlus related topics: Cesarean Section
U.S. FDA Resources

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

Genders 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
Please refer to this study by its ClinicalTrials.gov identifier: NCT00416104

Contacts
Contact: etan z zimmer, md 97248542652 e_zimmer@rambam.health.gov.il

Locations
Israel
Rambam Medical Center Not yet recruiting
Haifa, Israel, 31096
Contact: etan z zimmer, md     97248542652     e_zimmer@rambam.health.gov.il    
Principal Investigator: etan z zimmer, md            
Sponsors and Collaborators
Rambam Health Care Campus
Investigators
Principal Investigator: etan z zimmer, MD director of obstetrics rambam medical center
  More Information

No publications provided

ClinicalTrials.gov Identifier: NCT00416104     History of Changes
Other Study ID Numbers: zimmerctil
Study First Received: December 26, 2006
Last Updated: December 26, 2006
Health Authority: Israel: Israeli Health Ministry Pharmaceutical Administration

Keywords provided by Rambam Health Care Campus:
analgesia

ClinicalTrials.gov processed this record on May 23, 2013