Prolene Versus Ethibond for Cervical Cerclage



Status:Recruiting
Healthy:No
Age Range:18 - Any
Updated:10/19/2017
Start Date:August 1, 2017
End Date:December 2018
Contact:Jenani S Jayakumaran, MD
Email:jsjayakumaran@gmail.com
Phone:7327130092

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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 trial. Ethibond is another commonly used suture material for performing
cervical cerclage that shares some characteristics with previously studied suture materials.
It is braided like the Mersilene, but thinner like the monofilament Prolene. The
investigators will study whether Ethibond causes the vaginal microbiome to be adversely
affected like Mersilene or whether there is a healthy microbiome like Prolene. This study
will allow the investigators to determine whether it is advisable to continue to use Ethibond
for cervical cerclage in clinical practice, or whether obstetricians should avoid its use as
now done with Mersilene.


Inclusion Criteria:

- 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 Criteria:

- younger than 18 years of age

- multiple gestation

- iatrogenic preterm delivery

- pregnancies with fetal anomalies
We found this trial at
2
sites
125 Paterson Street
New Brunswick, New Jersey 08901
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mi
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New Brunswick, NJ
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125 Paterson Street
New Brunswick, New Jersey 08901
?
mi
from
New Brunswick, NJ
Click here to add this to my saved trials