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Comparing the efficacy of Ibuprofen and Celecoxib on the intensity of perineal pain following episiotomy

Phase 3
Conditions
post episiotomy pain.
Other complications of obstetric surgery and procedures
Registration Number
IRCT201106136790N1
Lead Sponsor
Ilam University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
170
Inclusion Criteria

1-18-35 y/o; 2-mediolateral episiotomy; 3-singleton; 4- alive fetus. Exclusion criteria: 1-sensitivity to NSAIDs; 2-history of digestive system disorders; 3-presence of chronic illness; 4-rupture of cervix; 5-post partum hemorrhage; 6-pre eclampcia and eclampcia; 7-PROM.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain severity. Timepoint: pre intervention,1, 2, 4, 8 and 12 hours after intervention. Method of measurement: VAS.
Secondary Outcome Measures
NameTimeMethod
Digestive system complications. Timepoint: Every 12 hours. Method of measurement: History and Physical exam.
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