Skip to main content
Clinical Trials/IRCT138903121096N3
IRCT138903121096N3
Completed
Phase 2

Comparison of Sublingual and vaginal Misoprostol for labor induction in primiparous women

Vice chancellor for research -Guilan university of medical sciences0 sites126 target enrollmentTBD

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
labour induction.
Sponsor
Vice chancellor for research -Guilan university of medical sciences
Enrollment
126
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

No summary available.

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

Investigators

Sponsor
Vice chancellor for research -Guilan university of medical sciences

Eligibility Criteria

Inclusion Criteria

  • a) single pregnancy (between 36 to 42 weeks), b) vertex presentation, c) intact fetal membrane, d) bishop score equal or less than four e) absence of uterus spontaneous contractions f) fetal weight less than 4000gr j) normal fetal heart rate h) cephalopelvic proportion Exclusion criteria: a) sensitivity to PGs b) previous history of cesarean c) uterus wall scar d) preeclampsia or blood pressure more than 140/90 mmhg e) PROM f) vaginal bleeding

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

Similar Trials