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RECRUITING
NCT06036446
NA

LATe Cerclage in High-risk Pregnancies (LATCH)

Sponsor: Thomas Jefferson University

View on ClinicalTrials.gov

Summary

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.

Official title: Cervical Cerclage for Short Cervix at 24-26 Weeks of Gestation: a Randomized Controlled Trial

Key Details

Gender

FEMALE

Age Range

18 Years - 50 Years

Study Type

INTERVENTIONAL

Enrollment

329

Start Date

2023-11-10

Completion Date

2029-02

Last Updated

2026-05-29

Healthy Volunteers

Yes

Conditions

Interventions

PROCEDURE

Cervical cerclage

Transvaginal cervical cerclage placed between 24 0/7 - 26 6/7 weeks of gestation.

DRUG

Vaginal Suppository Progesterone

Continuing or initiation of vaginal progesterone 200mg daily until 36 weeks of gestation.

Locations (2)

Atrium Health Carolinas Medical Center

Charlotte, North Carolina, United States

Thomas Jefferson University

Philadelphia, Pennsylvania, United States