Cervical length measurements in management of preterm labor: a randomized trial

Phase 3

• Conditions: Preterm labour / threatened preterm labour; Cervical length, threatened preterm labor, preterm labor, tocolysis, randomized trial

• Registration Number: TCTR20190821001
• Lead Sponsor: donthani hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2019-08-21
• Study Completion: 2019-08-31
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Enrolling by invitation
• Sex: Female
• Target Recruitment: 116

Inclusion Criteria

women with singleton live preterm (GA 25-36 weeks) pregnancies, have regular uterine contraction

Exclusion Criteria

women with placenta previa, abnormal vaginal bleeding, preterm premature rupture of membranes, cervical dilated more than 3 cm, Dead Fetus In Utero (DFIU), fetal anomaly,uncertained date of gestational age, have history of previous cervical or uterine surgery such as previous cesarean section or LEEP

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The success of inhibition labor within 48 hours admission date until delivery The period after the cervical length measurement and tocolytics drug administration

Secondary Outcome Measures

Name	Time	Method
maternal and neonatal outcome after delivery period analyzed data of maternal and neonatal outcome after delivery