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Clinical Trials/IRCT138706051096N1
IRCT138706051096N1
Completed
Phase 3

Evaluation of the effect of vaginal Progesterone in preventing preterm labor

Vice Chancellor for research-Guilan University of Medical Sciences0 sites260 target enrollmentTBD

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
prevention of preterm labor.
Sponsor
Vice Chancellor for research-Guilan University of Medical Sciences
Enrollment
260
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

  • Pregnant women were eligible to enter the trial if 1\) they were between 26\-36 weeks of gestation based on their LMP or sonography before 16 weeks of gestation. 2\) Confirmation of premature delivery with a)uterine contractions more than 30 seconds and three or more contractions per 30 minutes established by tochodynamometer b) cervical dilatation of 0\-2 cm in nulliparous and 1 \-2 cm in multiparous and cervical effacement greater than 50% 3\) intact membrane.
  • Exclusion criteria included: 1\) unwillingness or inability to comply with study procedures before 36 weeks of gestation 2\) lack of useful sufficient data 3\) preeclampsia requiring termination of pregnancy.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

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