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NCT02033304 Clinical Trial

Factors Predicting Postoperative Cesarean Section Pain

Postoperative Pain Clinical Trial

Official title:
Analysis of Factors Predicting Postoperative Pain and Wound Hyperalgesia After Cesarean Section

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02033304
Other study ID # 7124
Secondary ID
Status Completed
Phase N/A
First received January 9, 2014
Last updated May 6, 2015
Start date February 2014
Est. completion date July 2014

Study information
Verified date January 2013
Source Rabin Medical Center
Contact n/a
Is FDA regulated No
Health authority Israel: Israel health registry
Study type Observational

Clinical Trial Summary

In spite of identical analgesic protocols, parturients suffer different levels of pain postoperative lay. In this study we hope to identify factors which influence the perception of pain including preoperative anxiety, sleep quality and local anesthesia injection pain.

Recruitment information / eligibility
Status Completed
Enrollment 229
Est. completion date July 2014
Est. primary completion date July 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- Women undergoing spinal anesthesia

Exclusion Criteria:

- women unable to cooperate

- Women undergoing general anesthesia

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
Israel Beilinson hospital Petach tikvah
Israel Rabin medical center Petach tikvah

Sponsors (1)
Lead Sponsor Collaborator
Rabin Medical Center

Country where clinical trial is conducted

Israel, 

Outcome
Type Measure Description Time frame Safety issue
Primary Postoperative pain Postoperative day1 No
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