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Clinical Trials/CTRI/2015/01/005467
CTRI/2015/01/005467Active, not recruiting未知

Comparison of vaginal and intramuscular routes of progesterone delivery in prevention of preterm delivery in women with prior preterm birth

Postgraduate Institute of Medical Education and Research0 sites100 target enrollmentStarted: TBDLast updated:

Trial Snapshot

Phase
未知
Status
Active, not recruiting
Enrollment
100

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Inclusion Criteria

  • 1. Women with a singleton pregnancy between 16 to 24 weeks
  • 2. Women with at least one spontaneous second trimester abortion or preterm birth ( >16 weeks to <37 weeks) of a singleton infant due to spontaneous preterm labour or pProm

Exclusion Criteria

  • 1. Multifetal Gestation
  • 2. Known allergy to progesterone.
  • 3. Women with known medical disorders (Chronic Hypertension, Diabetes mellitus, heart disease) which may need preterm delivery
  • 4. Lethal congenital malformation of the fetes

Investigators

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