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Clinical Trials/IRCT201012035294N1
IRCT201012035294N1CompletedPhase 2

To investigate the possible effect of Progesterone Supp on cytokines endocervical concentration of women at risk of abortion

Vice chancellor for research,Tehran University of Medical Sciences0 sites100 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
Phase 2
Status
Completed
Sponsor
Enrollment
100

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
16 years to 44 years (—)
Sex
Female

Inclusion Criteria

  • pregnant women less than 20 weeks of gestation with sign and symptoms of threatened abortion like bleeding, abdominal pain and induction of cervical secretion where included in this study; Exclusion criteria: Lack of satisfaction, hypertension and avoidance of participating in the study were considered as exclusion criteria.

Exclusion Criteria

  • Not provided

Investigators

Sponsor
Vice chancellor for research,Tehran University of Medical Sciences

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