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Clinical Trials/IRCT20201115049389N1
IRCT20201115049389N1
Recruiting
Early Phase 1

Comparison of the effect of vaginal consumption of primrose oil on the preparation of cervix in term delivery at patient resort to educational hospitals of Medical Sciences

Mashhad University of Medical Sciences0 sites76 target enrollmentTBD
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Overview

Phase
Early Phase 1
Intervention
Not specified
Conditions
Not specified
Sponsor
Mashhad University of Medical Sciences
Enrollment
76
Status
Recruiting
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

  • •Low risk of pregnancy
  • •Bishop score less than 4
  • •BMI between 19 and 25
  • •Lack of systemic disease
  • •No drug addiction
  • •No vaginal bleeding
  • •Gain conscious satisfaction

Exclusion Criteria

  • •Patient non\-cooperation
  • •Increased risks of delivery
  • •Use other methods of uterine preparation
  • •Diabetes and hypertension
  • •Chronic inflammatory disease
  • •Improper fetal presentation

Outcomes

Primary Outcomes

Not specified

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