At a glance
ClinicalIndex Comparison RecordN/ACompleted· 385 enrolled
Drug / intervention
Silicon ring (Arabin Pessary)device
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Randomized Controlled Trial: Prevention of Preterm Birth Using Cervical Pessary in Pregnant Women With Short Cervix (PECEP)
In Brief
A clinical study evaluating Silicon ring (Arabin Pessary) for Preterm Birth. Completed, enrolled 385 participants across 6 sites.
Detailed Summary
Placement of a vaginal pessary reduces significantly the rate of spontaneous preterm birth in pregnant women with short cervical length at 18-22 weeks scan.
Study Details
Timeline
N/ACompletedFinished
200720082009201020112012201320142015201620172018201920202021202220232024202520262027
Enrollment StartJun 2007
First PostedJun 2008
Primary CompletionJul 2014
TodayJul 2026
First PostedJun 27, 2008
Enrollment StartJun 1, 2007
Primary CompletionJul 1, 2014
TodayJul 2, 2026
Enrollment to primary: 7.1 yearsPosted 18.0 years ago
Interventions
Silicon ring (Arabin Pessary)device
Placement of a silicon pessary in the vagina, around the cervix.