Vaginal Progesterone to Prevent Early Preterm Birth In Twin Pregnancy With Short Cervix. Double-Blind, Placebo-Controlled, Randomized Clinical Trial
Vaginal Progesterone to Prevent Early Preterm Birth In Twin Pregnancy With Short Cervix. Double-Blind, Placebo-Controlled, Randomized Clinical Trial
A Multicenter, Double-Blind, Placebo-Controlled Randomized Clinical Trial of Vaginal Progesterone to Prevent Early Preterm Birth In Twin Pregnancy with Short Cervix.
This is a placebo-controlled, double-blind, randomized clinical trial of asymptomatic women with twin pregnancy and a cervix length 10 mm to 25 mm discovered on a routine screening transvaginal sonogram between 20w0d to 24w0d gestational age. Women will be randomized in either the in-patient or out-patient setting (1:1) to a daily vaginal application of micronized progesterone cream(200 mg)vs. placebo to determine if daily vaginal progesterone administration reduces the risk of preterm birth prior to 34w0d of gestation.
Inclusion Criteria:
Exclusion Criteria:
Mother less than 18 years of age
Uterine contractions of 40 seconds duration or more, 10 or more per hour
Rupture of fetal membranes (leakage of amniotic fluid one or both sacs)
Ongoing vaginal bleeding
Any condition likely to cause serious neonatal morbidity independent of gestational age, including:
Any contraindication to continuing the pregnancy
Cervical cerclage in place or planned
Any contraindication to vaginal micronized progesterone, including: