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Clinical Trials/IRCT20180819040830N3
IRCT20180819040830N3
Completed
未知

Comparison of Efficacy and Safety of Cervical Pessary with Routine Management in Decreasing the Preterm Labor Rate in Nulliparous Symptomatic Pregnant Women with Short Cervix: A Randomized Clinical Trial

Shahid Beheshti University of Medical Sciences0 sites100 target enrollmentTBD
Conditionspreterm labor.

Overview

Phase
未知
Intervention
Not specified
Conditions
preterm labor.
Sponsor
Shahid Beheshti University of Medical Sciences
Enrollment
100
Status
Completed
Last Updated
5 years ago

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

  • Gestational age between 24 weeks and 0 days to 34 weeks and 0 days
  • Shortened cervical length (defined as cervical length \=25 mm measured by trans\-vaginal ultrasound scan in second trimester)

Exclusion Criteria

  • Major fetal abnormalities
  • Fever or any other clinical findings in favor of chorioamnionitis and
  • Placenta previa
  • Women with normal cervical length
  • Women who had not responded to the routine standard treatments of preterm labor and were experiencing continued signs and symptoms of preterm labor after 48 hours of admission
  • Vaginal bleeding
  • Signs of ruptured membranes.

Outcomes

Primary Outcomes

Not specified

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