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Clinical trials of Comparison the effect of two methods, patient controlled analgesia and non steroidal anti inflammatory drugs after elective cesarean sectio

Phase 2
Conditions
postoperative pain.
-
Registration Number
IRCT2014091619197N1
Lead Sponsor
Investigator
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
100
Inclusion Criteria

age between 20 to 35, no history of cesarean surgery, not suffering from chronic pain, BMI less than 30, no sensitivity to opioids drugs, chronic diseases and patient's written consent.
Exclusion criteria: a history of addiction to opioids, history of liver and kidney diseases, the existence of mental illness verifiy by a physician and lack of interest or withdrawal during the conduction of the study.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain intensity. Timepoint: every 6 hours after intervention. Method of measurement: visual analog scale.
Secondary Outcome Measures
NameTimeMethod
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