search
Back to results

Cervical Cerclage for Preventing Spontaneous Preterm Birth in Singleton Pregnancies Without Prior Spontaneous Preterm Birth and With Short Transvaginal Ultrasound Cervical Length

Primary Purpose

Preterm Birth

Status
Unknown status
Phase
Phase 4
Locations
Italy
Study Type
Interventional
Intervention
Cervical cerclage
Sponsored by
Federico II University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Preterm Birth

Eligibility Criteria

18 Years - 50 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • 18-50 ages
  • Singleton pregnancy
  • Cervical length <=25mm between 18(0) and 23(6) weeks

Exclusion Criteria:

  • Multiple pregnancy
  • Prior spontaneous preterm birth or second trimester losses between 16(0) and 36(6) weeks
  • Cerclage in situ
  • Painful regular uterine contraction and/or preterm labor
  • Ruptured membranes
  • Major fetal defects
  • Active vaginal bleeding
  • Placenda previa and/or accreta
  • Cervical dilation >1.5 cm and/or visible membranes by pelvic exam
  • Suspicion of chorioamnionitis

Sites / Locations

  • Gabriele SacconeRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Cervical cerclage

No intervention

Arm Description

After the woman is placed in the dorsal lithotomy position and the bladder is emptied with a urinary catheter to reduce the chance of bladder injury, surgical preparation with Betadine will be performed. Breisky retractors and Sims retractors will be used to exposure the entire cervix. Sponge ring forceps will be used to optimized visualization of the cervix and provide the necessary countertraction at the suture entry and exit sites. McDonald technique will be performed placing 4-6 bites circumferentially around the cervix. Only one stitch will be used. The suture will be places as high as feasible

Bed rest will be not recommended.

Outcomes

Primary Outcome Measures

Spontaneous preterm birth (SPTB)

Secondary Outcome Measures

Spontaneous preterm birth (SPTB)
Gestational age at delivery
mean gestational age at delivery in weeks
Latency
mean latency in days (from randomization to delivery)
chorioamnionitis
chorioamnionitis histologically proven
Birth weight
in grams
Admission to neonatal intensive care unit
respiratory distress syndrome
low birth weight
birth weight <2500 grams
intraventricular hemorrhage
grade 3 or 4
neonatal mortality
death of a live-born baby within the first 28 days of life

Full Information

First Posted
April 8, 2016
Last Updated
April 18, 2016
Sponsor
Federico II University
search

1. Study Identification

Unique Protocol Identification Number
NCT02746900
Brief Title
Cervical Cerclage for Preventing Spontaneous Preterm Birth in Singleton Pregnancies Without Prior Spontaneous Preterm Birth and With Short Transvaginal Ultrasound Cervical Length
Official Title
Cervical Cerclage for Preventing Spontaneous Preterm Birth in Singleton Pregnancies Without Prior Spontaneous Preterm Birth and With Short Transvaginal Ultrasound Cervical Length
Study Type
Interventional

2. Study Status

Record Verification Date
April 2016
Overall Recruitment Status
Unknown status
Study Start Date
April 2016 (undefined)
Primary Completion Date
April 2018 (Anticipated)
Study Completion Date
April 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Federico II University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Spontaneous preterm birth (SPTB) remains the number one cause of perinatal mortality in many countries, including the United States. In singleton gestations a short cervical length (CL) on transvaginal ultrasound (TVU) has been shown to be a good predictor of SPTB. Different strategies have been adopted for prevention of SPTB. Growing interest has focused on pessary for prevention of SPTB. Cervical pessary is relatively non-invasive, easy to use, does not require anesthesia, can be used in an outpatient clinic setting, and it is easily removed when necessary. However, a recent systematic review and meta-analysis of randomized clinical trials showed that in singleton pregnancies with short cervix, prophylactic use of the pessary did not reduce the rate of spontaneous preterm delivery or improve perinatal outcome. The evidence supports the use of vaginal progesterone in singleton pregnancies with short cervix, while cervical cerclage seems to be beneficial only in the subgroup of women with both prior SPTB and TVU CL ≤25mm. Interestingly, only 235 singletons without prior SPTB,7 and 504 singletons gestations with prior SPTB,6 have been included in randomized studies on cerclage for TVU CL ≤25mm. A meta-analysis of four trials showed that cervical cerclage did not prevent SPTB in women with short TVU CL and without prior preterm birth.7 However, even if the statistical significance were not reached, they found a reduction in SPTB <35 weeks by 16% in singletons with short TVU CL and without prior SPTB (20.6% vs 31.2%; relative risk (RR) 0.84, 95% confidence interval (CI) 0.60 to 1.17) and by 24% in singletons without risk factors for SPTB (25.6% vs 33.3%; RR 0.76, 95% CI 0.52 to 1.15). Therefore, the aim of this study is to evaluate the efficacy of cervical cerclage in prevention of SPTB in singleton pregnancies with short TVU CL in second trimester, without prior SPTB.
Detailed Description
Investigators aim to conduct a prospective, multicenter, randomized, open-label, clinical trial at Department of Reproductive Science, University of Naples Federico II. All women included in the study will provide a written informed consent to participate in the study before the randomization. Women with TVU CL ≤25mm who will meet the inclusion criteria will be counselled by an obstetrician regarding the risk of SPTB as per standard of care. The patient will be given ample time to have all questions addressed and consider participation. If the patient agrees to participate in the study, the informed consent form will be signed and a copy will be given to the patient. Women who are eligible and consent to participate in the study will be randomly assigned to one of two groups: cervical cerclage (i.e. intervention group) or standard obstetric management (i.e. control group). Investigators planned subgroup analyses according to different CL cutoffs (i.e. <=15 and <=10 mm); type of suture; and according to prior history of cervical surgery (i.e. LEEP or cone biopsy).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Preterm Birth

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
587 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Cervical cerclage
Arm Type
Experimental
Arm Description
After the woman is placed in the dorsal lithotomy position and the bladder is emptied with a urinary catheter to reduce the chance of bladder injury, surgical preparation with Betadine will be performed. Breisky retractors and Sims retractors will be used to exposure the entire cervix. Sponge ring forceps will be used to optimized visualization of the cervix and provide the necessary countertraction at the suture entry and exit sites. McDonald technique will be performed placing 4-6 bites circumferentially around the cervix. Only one stitch will be used. The suture will be places as high as feasible
Arm Title
No intervention
Arm Type
No Intervention
Arm Description
Bed rest will be not recommended.
Intervention Type
Procedure
Intervention Name(s)
Cervical cerclage
Intervention Description
McDonald cervical cerclage
Primary Outcome Measure Information:
Title
Spontaneous preterm birth (SPTB)
Time Frame
Less than 35 weeks gestation
Secondary Outcome Measure Information:
Title
Spontaneous preterm birth (SPTB)
Time Frame
Less than 37,34,32,28 and 24 weeks gestation
Title
Gestational age at delivery
Description
mean gestational age at delivery in weeks
Time Frame
Delivery (at birth)
Title
Latency
Description
mean latency in days (from randomization to delivery)
Time Frame
Delivery (at birth)
Title
chorioamnionitis
Description
chorioamnionitis histologically proven
Time Frame
Delivery (at birth)
Title
Birth weight
Description
in grams
Time Frame
Delivery (at birth)
Title
Admission to neonatal intensive care unit
Time Frame
Delivery (at birth)
Title
respiratory distress syndrome
Time Frame
Delivery (at birth)
Title
low birth weight
Description
birth weight <2500 grams
Time Frame
Delivery (at birth)
Title
intraventricular hemorrhage
Description
grade 3 or 4
Time Frame
Between birth and 28 days of age
Title
neonatal mortality
Description
death of a live-born baby within the first 28 days of life
Time Frame
Between birth and 28 days of age

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 18-50 ages Singleton pregnancy Cervical length <=25mm between 18(0) and 23(6) weeks Exclusion Criteria: Multiple pregnancy Prior spontaneous preterm birth or second trimester losses between 16(0) and 36(6) weeks Cerclage in situ Painful regular uterine contraction and/or preterm labor Ruptured membranes Major fetal defects Active vaginal bleeding Placenda previa and/or accreta Cervical dilation >1.5 cm and/or visible membranes by pelvic exam Suspicion of chorioamnionitis
Facility Information:
Facility Name
Gabriele Saccone
City
Napoli
ZIP/Postal Code
80129
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gabriele Saccone
Phone
339468517
Email
gabriele.saccone@libero.it

12. IPD Sharing Statement

Learn more about this trial

Cervical Cerclage for Preventing Spontaneous Preterm Birth in Singleton Pregnancies Without Prior Spontaneous Preterm Birth and With Short Transvaginal Ultrasound Cervical Length

We'll reach out to this number within 24 hrs