A Randomized Trial of Pessary in Singleton Pregnancies with a Short Cervix
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- STATUS
- Recruiting
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- participants needed
- 100
Summary
Preterm birth is the primary driver of perinatal morbidity and mortality affecting approximately 11% of all newborns in the United States.1 Of the 4 million neonatal deaths that occur annually around the world, more than a quarter are the result of preterm birth.2 A short cervix by ultrasound has been noted to be one of the strongest predictors of subsequent preterm birth and investigators have focused efforts in finding a treatment for women with a short cervix that will reduce the risk of preterm delivery. Although vaginal progesterone and cerclage have been shown to reduce the risk, results have not been uniformly positive, and a low-cost, simple and effective method would be of great value, especially globally. The cervical pessary is such a treatment. This randomized trial will evaluate whether a cervical pessary can reduce the risk of preterm birth before 37 weeks in women with a short cervix.
Details
| Condition | ['Short Cervix', 'Preterm Delivery'] |
|---|---|
| Age | 99years or below |
| Clinical Study Identifier | TBD |
| Last Modified on | 19 February 2024 |
Eligibility
How to participate?
Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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