ClinicalTrials.Veeva

Menu

Prevention of Preterm Birth Using Cervical Pessary in Pregnant Women With Short Cervix in Twins (PECEP-TWINS)

M

Maternal-Infantil Vall d´Hebron Hospital

Status and phase

Completed
Phase 4

Conditions

Preterm Birth

Treatments

Device: Silicon ring (Arabin Cervical Pessary)

Study type

Interventional

Funder types

Other

Identifiers

NCT01242410
Pessary in twins TRIAL

Details and patient eligibility

About

Placement of a vaginal pessary reduces significantly the rate of spontaneous preterm birth in pregnant women with twins and a short cervical length at 18-22 weeks scan.

Full description

This trial includes pregnant women with twins undergoing routine ultrasound examination at 18.0 to 22.6 weeks of gestation.

Enrollment

137 patients

Sex

Female

Ages

18 to 45 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Twins
  • Minimal age of 18 years

Exclusion criteria

  • Major fetal abnormalities (requiring surgery or leading to infant death or severe handicap)
  • Spontaneous rupture of membranes at the time of randomization
  • Cervical cerclage in situ
  • Active vaginal bleeding
  • Placenta previa

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

137 participants in 2 patient groups

Expectant Management
No Intervention group
Placement of cervical pessary since 23 weeks until 37 weeks
Experimental group
Treatment:
Device: Silicon ring (Arabin Cervical Pessary)

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems