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Clinical Trials/IRCT20201108049300N1
IRCT20201108049300N1Recruiting未知

Evaluation of the effect of oral probiotics on the prevention of preterm delivery in mothers at risk of preterm delivery compared with placebo

Yasouj University of Medical Sciences0 sites120 target enrollmentStarted: TBDLast updated:

Trial Snapshot

Phase
未知
Status
Recruiting
Sponsor
Enrollment
120

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
18 years to 45 years (—)
Sex
Female

Inclusion Criteria

  • Patient age 18-45 years
  • Gestational age between 16-24 weeks
  • Absence of syphilis, gonorrhea and HIV clinically
  • Having risk factors for preterm delivery in the current pregnancy, including a history of preterm delivery or a second trimester abortion in a previous pregnancy
  • No elective or emergency cerclage
  • Lack of maternal insulin-dependent diabetes mellitus, treatment of hypertension, lupus

Exclusion Criteria

  • Reluctance to participate in the study
  • Failure to complete the course of treatment or use of probiotics
  • Taking drugs that affect the intestinal microbial flora, such as antibiotics
  • Occurrence of any genital or urinary tract infection requires antibiotic treatment during treatment
  • Fetus with congenital malformations and abnormal scan anomalies
  • Clinical chorioamnionitis

Investigators

Sponsor
Yasouj University of Medical Sciences

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