Comparison of Extra-amniotic dexamethasone infusion with extra-amniotic salin infusion in cervical ripening for labor inductio

Phase 3

Recruiting

• Conditions: Pregnant wemen.; Z33; Pregnant s

• Registration Number: IRCT20190107042266N2
• Lead Sponsor: Semnan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 24 February 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 60

Inclusion Criteria

Gestational age of 37-42 weeks
Candidate for induction of labor
Bishop score of less than 5

Exclusion Criteria

Uterine anomalies
Placenta previa or placental low lying
Authentic History of vaginal bleeding in the second and third trimester of pregnancy
Active genital herpes
Intrauterine fetal death (IUFD)
History of uterine classic incision
Vasa Previa

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Cervical ripening. Timepoint: The measurement of cervix at the beginning of the study and before initiation of the intervention (until 6 hours after initiation of the study) till the creation of bishop score of five and higher. Method of measurement: Vaginal exam based on Bishop score.

Secondary Outcome Measures

Name	Time	Method
eonatal Apgar. Timepoint: First and fifth minutes after birth. Method of measurement: Standard method.