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Clinical Trials/IRCT20230610058438N1
IRCT20230610058438N1RecruitingPhase 3

The effect of Achillea millefolium rectal suppositories on the prevention of postpartum hemorrhage and after pain

Yasouj University of Medical Sciences0 sites100 target enrollmentStarted: TBDLast updated:

Trial Snapshot

Phase
Phase 3
Status
Recruiting
Sponsor
Enrollment
100

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
55 years to 15 years (—)
Sex
Female

Inclusion Criteria

  • Entry criteria: written consent to participate in the study, being Iranian, reading and writing, mother's age range between 15-50, desire to have natural childbirth, cephalic presentation, singleton pregnancy,
  • Term pregnancy (38 to 42 full weeks based on LMP or first trimester ultrasound)
  • Obtaining a score equal to or greater than 10% of the nemogram is the prevention of postpartum hemorrhage

Exclusion Criteria

  • Exclusion criteria include: allergy to yarrow, unwillingness to continue participating in the study, cesarean delivery, history of uterine surgery, use of herbal or chemical drugs before delivery and during labor and delivery.
  • The occurrence of serious complications after childbirth (higher temperature equal to 38 degrees Celsius and higher blood pressure equal to 140/90) contracting a medical disease
  • Heavy bleeding during childbirth, 3rd and 4th degree tears, uterine and cervical tears, use of epidural anesthesia, shoulder dystocia, decollement, require invasive measures or drugs.

Investigators

Sponsor
Yasouj University of Medical Sciences

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