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Clinical Trials/IRCT20230404057817N1
IRCT20230404057817N1
Not yet recruiting
Phase 3

Comparison of the effect of misoprostol and evening primrose oil on cervical dilatation before hysteroscopic surgery

Qazvin University of Medical Sciences0 sites120 target enrollmentTBD
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ConditionsHysteroscopy.

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Hysteroscopy.
Sponsor
Qazvin University of Medical Sciences
Enrollment
120
Status
Not yet recruiting
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

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

Investigators

Eligibility Criteria

Inclusion Criteria

  • •Menopausal women or women of reproductive age with no history of normal vaginal delivery (NVD)
  • •Closure of the cervix

Exclusion Criteria

  • •Women with cervical structural abnormalities and a history of cervical insufficiency
  • •Women with Müller malformations
  • •Women with a history of conization
  • •Women with any contraindications to EPO or misoprostol (EPO or misoprostol contraindications such as seizures, asthma, high blood pressure, glaucoma, etc.)
  • •Women who have a history of failed hysteroscopy or D\&C due to severe cervical stenosis.

Outcomes

Primary Outcomes

Not specified

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