LATe Cerclage in High-risk Pregnancies (LATCH)
Recruiting
N/A
Interventional Study
Premature Birth
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 18 – 50
- Sex
- Female
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 329 (estimated)
- Sponsor
- Thomas Jefferson University · Other
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About This Trial
The goal of this clinical trial is to determine whether cervical cerclage reduces the risk of preterm birth in patients with a short transvaginal ultrasound (TVU) cervical length (CL) ≤25mm between 24 0/7-26 6/7 weeks.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* 18-50 years old, pregnant, assigned female at birth
* Singleton pregnancy
* TVU CL ≤25mm between 24 0/7 - 26 6/7 weeks of gestation
Exclusion Criteria:
* Initial multifetal gestation with subsequent multifetal pregnancy reduction, or selective fetal termination performed \>1…
Contacts