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Evaluation of the effect of evening primrose oil capsules on postpartum pain in multiparous wome

Phase 3
Recruiting
Conditions
Postpartum pain.
Encounter for maternal postpartum care and examination
Registration Number
IRCT20210217050394N1
Lead Sponsor
Mashhad University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
90
Inclusion Criteria

Being Iranian
mother age between 18-35 years
singleton pregnancy with gestational age 37-42 weeks
normal delivery
live and seemingly healthy baby
baby weight between 4000-2500 grams
Normal delivery gravid 3-5
No use of narcotics and spinal and epidural anesthesia during labor
No cesarean section or previous uterine surgery
The second and third stages of normal delivery
Absence of medical disease and no grade 3 and 4 perineal and vaginal tears
Lack of sensitivity to medicinal plants and acetaminophen
Start breastfeeding until the first two hours after delivery and continue breastfeeding
Pain intensity (based on visual scale) 4 and more within 2 hours after delivery

Exclusion Criteria

The mother's unwillingness to participation
Allergy to medicinal plants
Medical and midwifery problems
First pregnancy
Multiplication
Mother age should not be between 18-35

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Postpartum pain in multiparous women. Timepoint: Beginning and end of the study and during the first 24 hours of labor - every 8 hours - one hour before and one hour after the intervention. Method of measurement: McGill Pain Questionnaire and Visual Pain Scale (VAS).
Secondary Outcome Measures
NameTimeMethod
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