Effect of non-tocolyitc drugs to delivery of pregnant women with threatened preterm labour and cervical length > 25 millimeters : A randomized controlled trial

Phase 1

• Conditions: delivery; maternal and neonatal complication and hospital cost; threatened preterm labour, cervical length, non- tocolytic drug&#44

• Registration Number: TCTR20200617001
• Lead Sponsor: Faculty of Medicine, Siriraj Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2020-06-17
• Study Completion: 2022-06-09
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Pending (Not yet recruiting)
• Sex: Female
• Target Recruitment: 264

Inclusion Criteria

Pregnant women with gestational about 20 weeks - 36 weeks +6 days, regular uterine contraction at least 1 time in 10 minute or 4 times in 20 minutes or 8 times in 60 minutes and cervical length >, = 25 millimeters

Exclusion Criteria

Pregnant women who is < 18 years old, need emergency treatment of tocolyitc drugs, active bleeding, previous received tocolytic drugs, placenta previa, abruptio placentae, previous performed cervical cerclage and has caused of uterine contraction including fever, UTI, URI,etc.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
term delivery 18 months Gestational age at delivery

Secondary Outcome Measures

Name	Time	Method
maternal and neonatal complication, drug used, hospital cost 18 months gestational age at delivery