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Prophylactic Cerclage for Twin Pregnancy With Shortened Cervix

Protective Value of Cervical Cerclage Against Preterm Birth in Twin Pregnancy With Short Cervix. A Randomized Controlled Trial.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05338164
Enrollment
100
Registered
2022-04-21
Start date
2021-12-20
Completion date
2024-10-31
Last updated
2025-02-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Preterm Birth, Twin Pregnancy With Antenatal Problem, Cervical Shortening

Brief summary

This randomized controlled trial is aimed to evaluate pregnancy and neonatal outcomes in twin pregnancies, in which a cervical cerclage is placed due to the shortening of the cervix with or without visible fetal membranes.

Detailed description

Introduction 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 mortality.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 births.5 However, there is growing evidence of beneficial effect of applying cervical cerclage. Based on a few, small, controlled trials, cervical cerclage may extend the pregnancy, if it is applied to a cervix of less than 15 mm.6,7 Such practice is still in need for further validation by well-structured and powered randomized controlled trials. Rationale: Pregnant in twins with history suggesting cervical weakness and evidence of shortened cervix in the current pregnancy might get benefit from mechanical support by cervical cerclage in trial to reduce the risk of preterm birth.

Interventions

McDonald cervical cerclage will be applied using Mersaline braided tape with double needle. Single stitch (4 bites) will be applied as close as possible to the level of internal os. The Knot will be put either anterior or posterior according to the surgeon desire.

Sponsors

Zagazig University
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* Age between 18-45 years. * Dichorionic twins. * Transvaginal sonographic cervical length is \<25 mm with or without internal os dilatation ≥10 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.

Design outcomes

Primary

MeasureTime frameDescription
The incidence of preterm birth at ≤33+6, and ≤31+6 weeks with cervical length ≤25 mmImmediate reporting of cases at time of delivery through study completion, an average of 1 yearRate of preterm births stratified by gestational age inside the included women

Secondary

MeasureTime frameDescription
Subgroup analysis for the risk of preterm birth at ≤33+6, and ≤31+6 weeks with cervical length ≤15 mmImmediate reporting of cases at time of delivery through study completion, an average of 1 yearsubgroup analysis for rate of preterm births for very short cervix
The incidence of miscarriage.Immediate reporting of cases at time of miscarriage through study completion, an average of 1 yearrate of missed, inevitable and complete miscarriages
Incidence of cervico-vaginal infectionafter confirmation of infection through study completion, an average of 1 yearRate of infections diagnosed during pregnancy by patient complaint, clinical examination and confirmed by culture and sensitivity).
Neonatal outcomes in both groupsearly neonatal through study completion, an average of 1 yearRate of untoward early neonatal outcomes respiratory distress, IVH, necrotizing enterocolitis, sepsis, NICU admission

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026