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Single Versus Double Suture Cervical Cerclage to Prevent Preterm Birth

Primary Purpose

The Primary Outcome is Preterm Delivery Before 28 Weeks Gestational Age Compared to Women With One vs Two Cerclages Placed

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Double cerclage
Single cerclage
Sponsored by
Stony Brook University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for The Primary Outcome is Preterm Delivery Before 28 Weeks Gestational Age Compared to Women With One vs Two Cerclages Placed

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleAccepts Healthy Volunteers

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

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

Sites / Locations

  • Stony Brook UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Single Cerclage

Double Cerclage

Arm Description

Standard single cervical cerclage will be placed

Double cerclage placement

Outcomes

Primary Outcome Measures

Preterm delivery <28 weeks gestation
Birth occurring less than 28 weeks and 0 days

Secondary Outcome Measures

Preterm delivery <34 weeks gestation
Birth occurring less than 34 weeks and 0 days
Preterm delivery <37 weeks gestation
Births occurring less than 37 weeks and 0 days

Full Information

First Posted
January 29, 2021
Last Updated
October 26, 2022
Sponsor
Stony Brook University
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1. Study Identification

Unique Protocol Identification Number
NCT04742647
Brief Title
Single Versus Double Suture Cervical Cerclage to Prevent Preterm Birth
Official Title
Single Versus Double Suture Cervical Cerclage to Prevent Preterm Birth: Prospective Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Recruiting
Study Start Date
February 1, 2021 (Actual)
Primary Completion Date
July 1, 2023 (Anticipated)
Study Completion Date
July 1, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Stony Brook University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
The Primary Outcome is Preterm Delivery Before 28 Weeks Gestational Age Compared to Women With One vs Two Cerclages Placed

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
84 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Single Cerclage
Arm Type
Experimental
Arm Description
Standard single cervical cerclage will be placed
Arm Title
Double Cerclage
Arm Type
Experimental
Arm Description
Double cerclage placement
Intervention Type
Procedure
Intervention Name(s)
Double cerclage
Intervention Description
Two cervical cerlages will be placed
Intervention Type
Procedure
Intervention Name(s)
Single cerclage
Intervention Description
One cerclage will be placed
Primary Outcome Measure Information:
Title
Preterm delivery <28 weeks gestation
Description
Birth occurring less than 28 weeks and 0 days
Time Frame
through study completion, an average of 1 year
Secondary Outcome Measure Information:
Title
Preterm delivery <34 weeks gestation
Description
Birth occurring less than 34 weeks and 0 days
Time Frame
through study completion, an average of 1 year
Title
Preterm delivery <37 weeks gestation
Description
Births occurring less than 37 weeks and 0 days
Time Frame
through study completion, an average of 1 year

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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 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
Facility Information:
Facility Name
Stony Brook University
City
Stony Brook
State/Province
New York
ZIP/Postal Code
11794
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Deidre Lee
Phone
631-444-9324
Email
deidre.lee@stonybrookmedicine.edu
First Name & Middle Initial & Last Name & Degree
Diana Garretto, MD

12. IPD Sharing Statement

Plan to Share IPD
No

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Single Versus Double Suture Cervical Cerclage to Prevent Preterm Birth

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