Effect of oral probiotics on the prevention of preterm delivery

Not Applicable

Recruiting

• Conditions: preterm delivery.; Preterm labor with preterm delivery; O60.1

• Registration Number: IRCT20201108049300N1
• Lead Sponsor: Yasouj University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 1 November 2021

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 120

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

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Premature preterm birth (less than 34 weeks gestation). Timepoint: End of intervention. Method of measurement: Symptom.;Late preterm birth (34-37 weeks gestation). Timepoint: End of intervention. Method of measurement: Symptom.