Postcesarean Section Pain: Possible Demographic and Medical Predictors - Full Text View

Postcesarean Section Pain: Possible Demographic and Medical Predictors

This study is not yet open for participant recruitment.
Verified by Rambam Health Care Campus, July 2006

Sponsored by:	Rambam Health Care Campus
Information provided by:	Rambam Health Care Campus
ClinicalTrials.gov Identifier:	NCT00416104

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

MedlinePlus related topics:

Cesarean Section

U.S. FDA Resources

Study Type:	Observational
Study Design:	Cross-Sectional, Defined Population, Retrospective Study

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

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
	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

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

Keywords provided by Rambam Health Care Campus:

analgesia

Study placed in the following topic categories:

Pain

ClinicalTrials.gov processed this record on October 22, 2008