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Prophylactic Cervical Cerclage in Twin Pregnancies With Non-shortened Cervix

Z

Zagazig University

Status

Enrolling

Conditions

Cervical Cerclage
Twin Pregnancy, Antepartum Condition or Complication
Preterm Birth

Treatments

Procedure: Cervical cerclage

Study type

Interventional

Funder types

Other

Identifiers

NCT05334264
ZU-IRB #8084/17-10-2021

Details and patient eligibility

About

This randomized controlled trial is aimed to assess the protective value of prophylactic cervical cerclage against preterm birth in twin pregnancies with history of one or more preterm births without having cervical shortening in the current pregnancy.

Full description

Multiple pregnancies are high-risk pregnancies and usually associated with an increased risk of neonatal morbidity and mortality, mainly due to preterm births. Preterm births occur in 50% of twin pregnancies and the mean gestational age for delivery is 35.3 weeks. Ten percent of all twin births take place before 32 weeks of gestation.1 Preterm births are responsible for more than 70% of all neonatal and infant deaths.2 Prematurity can have serious consequences for the child, such as hearing difficulties, vision impairment, learning disabilities, reduced IQ, and cerebral palsy. A cervical length of ≤25 mm in twin pregnancies is a good predictor of a spontaneous preterm birth when measured around 24 weeks of gestation.3,4 Numerous interventions have been attempted in order to prevent preterm births in twin gestations, but until now, no intervention has been effective. Use of cerclage in twin pregnancies is controversial. Some experts claim that placing a cervical cerclage could increase the risk of preterm births5, Fuchs and Senat6 concluded that cervical cerclage in asymptomatic twins did not reduce the risk of PTB. This conclusion came depending on small sample sized randomized trail done on less than 50 patients.7 Available meta-analytic data remained of limited value in view of the few and small clinical studies that were included.

Although the current meta-analyses indicate the lack of efficacy of cerclage in twin pregnancies, data from the US Standard Certificate of Live Birth indicated that roughly 10% of triplets and 1.3% of twins are still receiving cerclage.8 Some authors compared the efficacy of cerclage in twin pregnancies and singleton pregnancies and showed that women with twin pregnancies who received cerclage might show beneficial obstetric outcomes similar to those of women with singleton gestations.9,10 Such practice is still in need for further validation by well-structured and powered randomized controlled trials.

Enrollment

170 estimated patients

Sex

Female

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age between 18-50 years.
  • Dichorionic twins.
  • History of ≥1 preterm birth.
  • Transvaginal sonographic cervical length is ≥25 mm at 14-20 weeks gestational age.
  • Asymptomatic.

Exclusion criteria

  • Triplets and quadruplets.
  • Monochorionic twins.
  • Threatened/ inevitable miscarriage
  • Bulging membranes through the external os.
  • Extremes of age.
  • Major fetal anomalies.
  • Known cases with uterine anomalies e.g. bicornuate uterus, uterus didelphis... etc.
  • Fetal demise.
  • Fetal reduction in the current pregnancy.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

170 participants in 2 patient groups

Group A
Experimental group
Description:
cervical cerclage between 14 and 20 weeks will be done by one of the three authors. McDonald cervical cerclage.
Treatment:
Procedure: Cervical cerclage
Group B
No Intervention group
Description:
Routine antenatal care without cerclage

Trial contacts and locations

1

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Central trial contact

Hytham Atia

Data sourced from clinicaltrials.gov

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