IRCT20210217050394N1RecruitingPhase 3
Evaluation of the effect of evening primrose oil capsules on postpartum pain in multiparous women
Trial Snapshot
- Phase
- Phase 3
- Status
- Recruiting
- Enrollment
- 90
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 18 years to 35 years (—)
- Sex
- Female
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
Investigators
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