Overview

Cerclage On LOw Risk Singletons: Cervical Cerclage for Prevention of Spontaneous Preterm Birth in Low Risk Singleton Pregnancies With Short Cervix

Status:
Recruiting
Trial end date:
2025-12-01
Target enrollment:
0
Participant gender:
Female
Summary
The aim of this study is to evaluate the efficacy of cervical cerclage in prevention of spontaneous preterm birth in singleton pregnancies with a short transvaginal cervical length (<=25mm) and without prior spontaneous preterm birth
Phase:
N/A
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Thomas Jefferson University
Treatments:
Progesterone
Criteria
Inclusion Criteria:

- 18 year old or older

- Singleton pregnancy

- No prior SPTB or second trimester losses between 160 and 366 weeks

- TVU CL ≤25mm between 180 and 236 weeks

Exclusion Criteria:

- Multiple pregnancy

- Prior SPTB or second trimester losses between 160 and 366 weeks

- Cerclage in situ

- Painful regular uterine contraction and/or preterm labor

- Rupture membranes

- Major fetal anomaly or aneuploidy

- Active vaginal bleeding

- Placenta previa and/or accreta

- Cervical dilation >1.0 cm and/or visible membranes by pelvic exam

- Suspicion of chorioamnionitis