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Clinical Trials/IRCT20201024049128N1
IRCT20201024049128N1
Recruiting
Phase 4

A Comparative Study about Maternal and Neonatal Outcomes of Using Extra-Amniotic Saline Infusion and vaginal Misoprostol for Cervical Ripening and Labor Induction in Pregnant Women with Unfavorable Cervix

Karaj University of Medical Sciences0 sites144 target enrollmentTBD
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Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Not specified
Sponsor
Karaj University of Medical Sciences
Enrollment
144
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

Sponsor
Karaj University of Medical Sciences

Eligibility Criteria

Inclusion Criteria

  • •Singleton gestation
  • •Alive fetus
  • •Cephalic presentation
  • •Intact membranes
  • •Unfavorable cervix (Bishopscore \=6\)
  • •Reassuring fetal heart rate
  • •Gestational age\=28

Exclusion Criteria

  • •Non\-cephalic presentation
  • •Adequate uterine contractions (3 contractions Lasting for 30sec/10 min)
  • •Ruptured membranes
  • •Cephalopelvic disproportion
  • •Multiple pregnancy
  • •Polyhydramnios
  • •Estimated fetal weight \=4000g or \=1800g
  • •Placental abruption, Placenta previa
  • •Unexplained vaginal bleeding
  • •Prior lower segment cesarean section/Scarred uterus

Outcomes

Primary Outcomes

Not specified

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