Oral probiotics and cerclage

Not Applicable

• Conditions: Cervical insufficiency.; Pregnancy with abortive outcome; O00-O08

• Registration Number: IRCT20160524028038N11
• 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: 7 February 2023

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 104

Inclusion Criteria

Patient age 18-45 years
Gestational age between 14-24 weeks
Cerclage by McDonald method
Absence of syphilis, gonorrhea and HIV clinically
Single pregnancy
Lack of maternal insulin-dependent diabetes mellitus, treatment of hypertension, lupus
No clinical chorioamnionitis

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

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: Questionnaire.;Late preterm birth (34-37 weeks gestation). Timepoint: End of intervention. Method of measurement: Questionnaire.;Premature rupture of amniotic sac,. Timepoint: End of intervention. Method of measurement: Questionnaire.;Type of delivery (normal and cesarean section). Timepoint: End of intervention. Method of measurement: Questionnaire.