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Single Versus Double Suture Cervical Cerclage to Prevent Preterm Birth

Not Applicable
Recruiting
Conditions
The Primary Outcome is Preterm Delivery Before 28 Weeks Gestational Age Compared to Women With One vs Two Cerclages Placed
Interventions
Procedure: Single cerclage
Procedure: Double cerclage
Registration Number
NCT04742647
Lead Sponsor
Stony Brook University
Brief Summary

Cerclage placement is known to be beneficial in prevention of preterm birth when placed inn a certain subset of patients. Clinically, the number of sutures can also vary by surgeon preference to one or two sutures in one procedure. This is often decided in the operating room (OR) on the day of surgery but is poorly studied in the efficacy of maintaining the closed cervical length. Retrospective data found no significant benefit on placing two stitches instead of one in preterm birth rate but was extremely limited and heterogenous in many clinical characteristic among the cerclage procedures. There were suggestions that two cerclage sutures may reduce the risk of cerclage revision, birth before 20 weeks, and a nonsignificant improvement in outcome of early preterm deliveries. Therefore, two randomized controlled trials, one prospective study and one meta-analysis were performed. They did suggest a beneficial effect of double cerclage on obstetrical outcomes especially in earlier preterm birth rates although all were limited in sample size and therefore power. A randomized control trial with adequate sample size is still needed to answer the question of whether double cervical cerclage suture is more beneficial than a single suture. Therefore, we propose conducting a randomized control trial between a single or double suture in prophylactic and ultrasound indicated cerclage procedures.

Detailed Description

Preterm birth (PTB), defined as birth at less than 37 completed weeks is the leading cause for neonatal mortality and morbidity in the USA. The most common risk factor for PTB is a prior preterm birth. The etiology includes several risk factors including prior preterm birth, cervical insufficiency, short cervical length, low socioeconomic and educational status, extremes of maternal age, genital tract infection/colonization, smoking, underlying chronic disease, uterine anomalies, cervical surgery, injury to the endometrium, race, and exposure to environmental factors. The objective of our study specifically focuses on cervical insufficiency and a short cervical length at \<24 weeks gestation defined as less than 25 mm as measured by transvaginal ultrasonography. It is well known that infants born prematurely have increased morbidity and mortality, including respiratory distress syndrome, intraventricular hemorrhage, necrotizing enterocolitis, long term health and neurologic abnormalities, extensive hospital stays, neonatal death, etc. The risks are significantly more pronounced at earlier gestational ages. Cervical cerclage, when indicated, has been shown to be beneficial in reducing preterm birth rates and therefore decrease adverse neonatal outcomes, perinatal morbidity, and mortality. The indications for cervical cerclage include a history of recurrent second trimester losses and/or PTB (history indicated), short cervical length (\<2.5cm on transvaginal ultrasound (ultrasound indicated), or a dilated cervix on physical exam (physical exam indicated). Our study focuses on history and ultrasound indicated cerclage.

There are various surgical approaches to placement of cervical cerclages- transvaginal and transabdominal. Our study focuses on the transvaginal approach and the modified McDonald technique with transvaginal placement of a purse-string suture at the cervicovaginal junction. Suture material varies by the surgeon's preference and can involve monofilament suture (Prolene), polyester fiber (Mersilene tape), or a braided polyester suture (Ti-Cron or Ethibond). Clinically, the number of sutures can also vary by surgeon preference to one or two sutures in one procedure. This is often decided in the operating room (OR) on the day of surgery but is poorly studied in the efficacy of maintaining the closed cervical length. Retrospective data found no significant benefit on placing two stitches instead of one in preterm birth rate but was extremely limited and heterogenous in many clinical characteristic among the cerclage procedures. There were suggestions that two cerclage sutures may reduce the risk of cerclage revision, birth before 20 weeks, and a nonsignificant improvement in outcome of early preterm deliveries. Therefore, two randomized controlled trials one prospective study and one meta-analysis were performed. They did suggest a beneficial effect of double cerclage on obstetrical outcomes especially in earlier preterm birth rates although all were limited in sample size and therefore power. A randomized control trial with adequate sample size is still needed to answer the question of whether double cervical cerclage suture is more beneficial than a single suture.

Recruitment & Eligibility

Status
RECRUITING
Sex
Female
Target Recruitment
84
Inclusion Criteria
  • 18 years of age and older
  • Confirmed intrauterine, live pregnancy
  • Singleton gestation
  • Cerclage indications including:
  • Prophylactic due to history of cervical insufficiency, second trimester loss
  • Ultrasound indicated short cervix <25 mm prior to 24 weeks
Read More
Exclusion Criteria
  • Rescue cerclage
  • Carrying a fetus with known aneuploidy or anomaly
  • Fetal demise
  • Clinical intra-amniotic infection
  • Rupture of membranes
  • Multiple gestation
  • Placental Abruption
  • Technique other than McDonald
  • Abdominal cerclage
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Single CerclageSingle cerclageStandard single cervical cerclage will be placed
Double CerclageDouble cerclageDouble cerclage placement
Primary Outcome Measures
NameTimeMethod
Preterm delivery <28 weeks gestationthrough study completion, an average of 1 year

Birth occurring less than 28 weeks and 0 days

Secondary Outcome Measures
NameTimeMethod
Preterm delivery <34 weeks gestationthrough study completion, an average of 1 year

Birth occurring less than 34 weeks and 0 days

Preterm delivery <37 weeks gestationthrough study completion, an average of 1 year

Births occurring less than 37 weeks and 0 days

Trial Locations

Locations (1)

Stony Brook University

🇺🇸

Stony Brook, New York, United States

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