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Clinical Trials/IRCT20201218049749N1
IRCT20201218049749N1
Completed
Phase 3

A comparison of vaginal misoprostol and vaginal evening primrose oil in first trimester termination

Kashan University of Medical Sciences0 sites72 target enrollmentTBD
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ConditionsSpontaneous abortion.Genital tract and pelvic infection following incomplete spontaneous abortionO03.0

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Spontaneous abortion.
Sponsor
Kashan University of Medical Sciences
Enrollment
72
Status
Completed
Last Updated
5 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
5 years ago
Study Type
Interventional
Sex
Female

Investigators

Eligibility Criteria

Inclusion Criteria

  • •Pregnant women go to Beheshti Hospital for up to 14 weeks to terminate their pregnancy

Exclusion Criteria

  • •Uncontrolled seizures
  • •Uncontrolled blood pressure
  • •Chronic lung disease
  • •Mitral valve stenosis
  • •History of known allergy to prostaglandin E1
  • •Inflammatory bowel disease
  • •Sensitivity to evening primrose
  • •Coagulation disease
  • •Schizophrenia and phenothiazine use
  • •Cone biopsy of the cervix

Outcomes

Primary Outcomes

Not specified

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