Comparison of efficacy of oral and vaginal progesterone to prevent preterm birth in pregnant women with short cervix: Randomized controlled trial

Phase 4

Completed

• Conditions: Preterm delivery; cervical length; progesterone

• Registration Number: TCTR20190324001
• Lead Sponsor: none

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Completion: 2018-08-20
• Study Start: 2019-03-24
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Female
• Target Recruitment: 84

Inclusion Criteria

All pregnancy with 20-25 weeks of gestation women who visited ANC clinic at SPS Hospital
A singleton
Cervical length 25 mm or less by transvaginal ultrasound measure

Exclusion Criteria

History of allergy of progesterone
Fetal anomaly
Fetal aneuploidy
Cervical incompetence

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
preterm birth before 34 weeks until the patients delivery medical record of labor at Suspasittiprasong Hospital,preterm birth before 37 weeks until the patients delivery medical record of labor at Suspasittiprasong Hospital

Secondary Outcome Measures

Name	Time	Method
maternal obstatic complication After discharge from Suspasittiprasong Hospital due to delivery medical record at Suspasittiprasong Hospital,neonatal complication After discharge from Suspasittiprasong Hospital due to delivery medical record at Suspasittiprasong Hospital,change in cervical length after progesterone was used 4 weeks after the first measure at date of enrollment measure by transvaginal ultrasound