Prediction and Prevention of Preterm Birth (PREVENT-PTB Study)

Preterm birth (PTB) remains the leading cause of neonatal mortality and long-term disability
throughout the world. Recently treatments early in pregnancy such as progesterone, cervical
support and maternal support have been demonstrated to delay delivery amongst at risk women.
Nonetheless, the majority of women who are at risk are not identified using current screening
methods.

Women who are 18 years or older, with a singleton pregnancy between 19 5/7 weeks and 20 6/7
weeks gestational age (GA) confirmed by ultrasound prior to enrollment and no history of
prior preterm birth (delivery between 16 0/7 weeks and 37 6/7 weeks) will be invited to
participate. Women who enroll will be randomized to screening and intervention for those at
high risk of PTB or no screening and standard care. All participants will undergo sample
collection, but the samples from the group randomized to "no screening' will not be analyzed
until the end of the study (post-delivery of all neonates).

Women randomized to the intervention group will be screened using the PreTRM® test (Sera
Prognostics, Inc.) at a large tertiary care center. Predicated upon the degree of risk, women
will be treated according to a pre-specified algorithm. The outcomes of these women will be
compared to a control group of women who do not receive screening at the same tertiary care
center.

Inclusion Criteria

1. Subject is greater than or equal to 18 years of age AND

2. Uncomplicated singleton intrauterine pregnancy less than 21 weeks estimated gestation
AND

3. No medical contraindications to continuing pregnancy AND

4. No previous classical cesarean section AND

5. No known uterine anomaly AND

6. No history of cervical conization AND

7. No plan for cesarean section prior to 37 0/7 weeks gestation AND

8. No plan for induction of labor prior to 37 0/7 weeks gestation AND

9. Subject has no history of spontaneous preterm delivery AND

10. No prior PPROM less than 34 weeks AND

11. Subject has no signs and/or symptoms of preterm labor AND

12. Subject has intact membranes AND

13. Subject has not received a blood transfusion during the current pregnancy.

Exclusion Criteria

1. Subjects who have taken or plan to take progesterone beyond 13 6/7 weeks gestation
prior to study enrollment OR

2. Any other medical conditions that put subject at increased risk of preterm birth in
the judgment of the site investigator OR

3. The subject has a planned cerclage placement for the current pregnancy OR

4. Previously identified short cervix (less than 2.5 cm by transvaginal ultrasound) prior
to enrollment OR

5. Known major structural fetal anomalies that may shorten pregnancy (e.g., anencephaly,
holoprosencephaly, schizencephaly, gastroschisis, omphalocele, congenital
diaphragmatic hernia) OR

6. Known fetal genetic anomalies that are incompatible with life (e.g., trisomy 13 or
trisomy 18) OR

7. The subject has known elevated bilirubin levels (hyperbilirubinemia) OR

8. The subject has taken or plans to take any of the following medications after the
first day of the last menstrual period: Enoxaparin, heparin, heparin sodium, low
molecular weight heparin, low dose aspirin OR

9. A history of allergic reaction to aspirin or 17-OHPC injections OR

10. Subject does not plan to deliver at an Intermountain Healthcare hospital.