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Progesterone for the Management of Preterm, Premature Rupture of the Membranes: A Randomized Controlled Trial.

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Stanford University

Status and phase

Completed
Phase 2
Phase 1

Conditions

Pregnancy Complications

Treatments

Drug: 17-Hydroxyprogesterone Caproate
Other: Caster Oil injections

Study type

Interventional

Funder types

Other

Identifiers

NCT01050647
SU-01082010-4683
17976 (Other Identifier)

Details and patient eligibility

About

Preterm birth is the leading cause of neonatal death and a significant cause of life long disability and health problems. It has been shown that the drug 17-hydroxyprogesterone caproate can help reduce the risk of preterm delivery in women with certain risk factors for preterm birth. We hope to learn whether this same medication can be used to prolong pregnancy in a group of patients in whom this medication has not been previously studied. Specifically, we hope to learn whether progesterone supplementation will delay delivery in women with pre-term, premature rupture of membranes (PPROM).

Full description

When women present to either the Obstetrical clinic or labor and delivery with a complaint of possible preterm, premature rupture of membranes (PPROM), they will be examined by an obstetrician to either confirm or rule out this diagnosis. If they are diagnosed with PPROM, they will then be admitted to Lucile Packard Children's Hospital and treated with the normal protocol which includes receiving antibiotics, receiving steroids, being hospitalized until delivery, and having ongoing maternal and fetal monitoring for possible complications. The patients will be identified by their treating obstetricians as possible study candidates and asked by a member of the treatment team if they are potentially interested in participating in a research study. Subsequently, a member of the study team or the treating physician will approach the patient about participating in the trial. Those who choose to participate will receive the standard care protocol in addition to receiving the study medication. The study medication will be a weekly injection of either placebo or 17-hydroxyprogesterone caproate or placebo. The placebo medication (castor oil) was chosen as it has been used in previous studies as a placebo for 17-hydroxyprogesterone caproate. The choice of which medication the patient receives will be determined by a randomization table. Only the pharmacist will be aware of the medication that has been administered. The patient, members of the treatment team, and members of the study team will be blinded to the medication that is being administered. The timing of their delivery will be managed by the treating obstetrician according to standard medical practice. After delivery, the patient's and her infant's medical outcomes will be recorded for analysis.

Enrollment

21 patients

Sex

Female

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. 18yr of age
  2. Singleton pregnancy
  3. PPROM confirmed on clinical exam
  4. GA between 24+0 and 33+5 wk
  5. Ability to understand consent in either English or Spanish

Exclusion criteria

  1. Contraindication to ongoing pregnancy including:

    1. Evidence of active infection
    2. Evidence of significant placental abruption
    3. IUFD diagnosed at the time of P-PROM diagnosis
  2. Major fetal malformation

  3. Maternal allergy to progesterone or placebo drug components

  4. Current use of progesterone at the time of P-PROM

  5. Multiple Gestations

  6. Inability to understand consent in either English or Spanish

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

21 participants in 2 patient groups, including a placebo group

17-hydroxyprogesterone caproate
Active Comparator group
Description:
Weekly injections of 17-hydroxyprogesterone caproate until patient reached 34 completed weeks of gestation
Treatment:
Drug: 17-Hydroxyprogesterone Caproate
Castor oil injections
Placebo Comparator group
Description:
Weekly injections of Caster Oil (placebo)
Treatment:
Other: Caster Oil injections

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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