Routine Activity and Preterm Delivery Risk in Women With a Short Cervix

Recruiting N/A Interventional Study
Cervical Shortening
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Sex
Female
Study type
Interventional
Purpose
Prevention
Participants needed
100 (estimated)
Sponsor
Wolfson Medical Center · Government
Think this trial could be right for you?

Answer a few quick questions to see if you may meet the eligibility requirements.

Check Your Eligibility
About This Trial
The goal of this clinical trial is to evaluate the effect of routine activity versus rest on the risk of preterm delivery in pregnant women with a short cervix diagnosed between 24 and 34 weeks of gestation. The main questions it aims to answer are: Does routine activity influence the gestational age at delivery? How does routine activity affect secondary outcomes such as preterm labor, premature…
Trial Locations
Loading…

Loading trial locations…

Eligibility Criteria
Inclusion Criteria: * Singleton pregnancies between 24+0 and 34+6 weeks. * Short cervical length (\<25 mm) confirmed via transvaginal ultrasound. * No medical contraindications to physical activity. Exclusion Criteria: * Twin pregnancies or higher-order multiples. * Medical indications for reduce…
Contacts

No contact information available.