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Effect of Eremostachys Laciniata suppository on post secarean section pain and distress

Phase 2
Recruiting
Conditions
Pain after cesarean section.
Pelvic and perineal pain
Registration Number
IRCT20150424021917N9
Lead Sponsor
Tabriz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
86
Inclusion Criteria

Women of childbearing age
Gestational age 39 weeks full
Body mass index (BMI) normal (25-19)
The lack of pairs of adhesions based on the Calledapel ultrasound

Exclusion Criteria

Unwilling to participate in the study
Having any underlying illness
Having gastric ulcer
Increase the duration of surgery for more than an hour
High-risk pregnancies
Damage to body tissues during cesarean section
Emergency Cesarean section

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain severity. Timepoint: Before intervention and after intervention (every 8 hours in the first 24 hours after cesarean section). Method of measurement: Visual Analog Scale (VAS).
Secondary Outcome Measures
NameTimeMethod
Perceived distress score after cesarean section. Timepoint: 24 hours after cesarean section. Method of measurement: Symptom Distress Scale.
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