Status:
COMPLETED
Prolene Versus Ethibond for Cervical Cerclage
Lead Sponsor:
Rutgers University
Conditions:
Cervical Incompetence
Eligibility:
FEMALE
18+ years
Phase:
NA
Brief Summary
The purpose of the proposed study is to examine the relationship between cerclage suture material of Ethibond and Prolene and its effect on the vaginal microbiome in a prospective randomized control t...
Eligibility Criteria
Inclusion
- Greater than18 years of age
- Singleton pregnancy
- History of preterm delivery between 17 0/7 weeks - 33 4/7 weeks with painless cervical
- dilation or cervical insufficiency
Exclusion
- younger than 18 years of age
- multiple gestation
- iatrogenic preterm delivery
- pregnancies with fetal anomalies
Key Trial Info
Start Date :
August 1 2017
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 31 2019
Estimated Enrollment :
16 Patients enrolled
Trial Details
Trial ID
NCT03311867
Start Date
August 1 2017
End Date
December 31 2019
Last Update
March 13 2020
Active Locations (2)
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1
Division of Maternal Fetal Medicine
New Brunswick, New Jersey, United States, 08901
2
High Risk Obstetrics Clinic
New Brunswick, New Jersey, United States, 08901