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Physical Exam Indicated Cerclage in Singleton Gestation 24 Weeks to 25 Weeks and 6 Days Gestation

Not Applicable
Conditions
Preterm Birth
Interventions
Procedure: Physical Exam Indicated Cerclage
Registration Number
NCT05501938
Lead Sponsor
Albany Medical College
Brief Summary

RCT assessing preterm delivery rate in singleton pregnancies having a physical-exam indicated cerclage placed between 24 weeks and 25 weeks and 6 days. Patients randomized to either cerclage intervention or routine standard of care (no cerclage).

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
Female
Target Recruitment
30
Inclusion Criteria
  1. Pregnant women 18 years of age or older
  2. Nulliparous patient, has not had a preterm to term delivery
  3. Singleton pregnancy
  4. English or Spanish speaking
  5. Asymptomatic cervical dilation between 1- 2 cm, without visible membranes beyond the external cervical os and without any evidence of infection, active labor or active bleeding between 24 0/7 and 25 6/7 weeks gestation
Exclusion Criteria
  1. Twin or higher order multi-fetal gestation

  2. Multiparous patient, has had one or more preterm to term deliveries

  3. Cervical dilation more than 2 cm either at the beginning of the study or any time during the study

  4. Amniotic membranes prolapsed beyond the external os

  5. Fetal reduction procedure performed during current pregnancy

  6. Ruptured membranes prior to randomization

  7. Major fetal structural anomaly

  8. Fetal chromosomal abnormality, suspected or confirmed with additional genetic testing

  9. Cerclage already in place for other indication

  10. Active vaginal bleeding

  11. Suspicion of chorioamnionitis

  12. Placenta previa

  13. Painful regular uterine contractions

  14. History of preterm birth before 37 weeks gestation

  15. Non-English or non-Spanish speaking

    a. Given that the study is explained in person and consent forms are written in English, there is no guarantee that the study will be explained correctly when using a phone translator. The same is true if the current English consent form were to be translated into a language other than English. There is no way to confirm that the integrity of the study is being upheld by using translating services. If the integrity of the study is not upheld, then this poses harm to the patient.

  16. Women under 18 years of age

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
CerclagePhysical Exam Indicated CerclagePerform physical exam indicated cerclage between 24w0d to 25w6d
Primary Outcome Measures
NameTimeMethod
Preterm Delivery Rate1 Year

Compare preterm delivery rate between women receiving cerclage intervention between 24w0d and 25w6d vs those not receiving cerclage during this gestational age period

Secondary Outcome Measures
NameTimeMethod
Neonatal Outcomes1 Year

Rate of neonatal outcomes compared between the two groups ( NICU length of stay, neonatal death, neonatal disease (bronchopulmonary dysplasia, Necrotizing enterocolitis, Intraventricular hemorrhage, Respiratory distress syndrome, Retinopathy of prematurity, sepsis, death)

Trial Locations

Locations (1)

Albany Medical Center

🇺🇸

Albany, New York, United States

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