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Clinical Trial

Effect of a Cervical Pessary on the Rate of Bleeding in Placenta Praevia

NCT: NCT07667777 · RECRUITING

NCT IDNCT07667777
StatusRECRUITING
Start Date2026-06
Completion2027-07
SponsorAsklepios proresearch (INDUSTRY)
First posted
Last updated

Brief Summary

This study evaluates whether use of a cervical pessary can reduce vaginal bleeding and prolong pregnancy in women with placenta previa or a low-lying placenta. Placenta previa is a condition in which the placenta covers or lies close to the cervix and may cause serious bleeding, preterm birth, and complications for both the pregnant woman and the baby. In this prospective, randomized, multicenter study, eligible women with singleton pregnancies and ultrasound-confirmed placenta previa or low-lying placenta between 20 and 30 weeks of gestation will be assigned either to treatment with an Arabin cervical pessary or to standard care without a pessary. The study will compare bleeding-related outcomes and pregnancy duration between the two groups. The study is designed to determine whether a cervical pessary is a safe and effective intervention for reducing bleeding-related complications and prolonging gestation in this high-risk pregnancy population.

Frequently Asked Questions

What is Effect of a Cervical Pessary on the Rate of Bleeding in Placenta Praevia?

Effect of a Cervical Pessary on the Rate of Bleeding in Placenta Praevia is a clinical trial registered under NCT07667777. Current status: RECRUITING.

What is the status of NCT07667777?

The current status of NCT07667777 (Effect of a Cervical Pessary on the Rate of Bleeding in Placenta Praevia) is: RECRUITING.

When did Effect of a Cervical Pessary on the Rate of Bleeding in Placenta Praevia start?

Effect of a Cervical Pessary on the Rate of Bleeding in Placenta Praevia started on 2026-06.

Official Source

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Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.