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

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

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20190821001
Enrollment
116
Registered
2019-08-21
Start date
2018-11-01
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Preterm labour / threatened preterm labour Cervical length&#44

Interventions

Cervical length (CL) measured in preterm labour pregnant and observe if CL > 3 cm ,Non cervical length measured in preterm labour pregnant and decide to tocolytocs administration if uterine contractio
cervical length measurement,Non cervical length measurement

Sponsors

Udonthani hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

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

Exclusion criteria

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

Design outcomes

Primary

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

Secondary

MeasureTime frame
maternal and neonatal outcome after delivery period analyzed data of maternal and neonatal outcome after delivery

Countries

Thailand

Contacts

Public ContactJirada Promnimit

Udonthani hospital

Jirada.note4@gmail.com+66902364535

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026