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Clinical Trials/NCT00946088
NCT00946088
Terminated
Phase 2

Progesterone for Maintenance Tocolysis: A Randomized Placebo Controlled Trial

Stanford University1 site in 1 country7 target enrollmentOctober 2009

Overview

Phase
Phase 2
Intervention
Progesterone
Conditions
Pregnancy Complications
Sponsor
Stanford University
Enrollment
7
Locations
1
Primary Endpoint
Reduction in Delivery Rate Prior to 37 Weeks Gestation
Status
Terminated
Last Updated
9 years ago

Overview

Brief Summary

Preterm delivery is the most common cause of infant morbidity and mortality in the United States. Some women have episodes of preterm labor during their pregnancy which can be temporarily stopped. These women, however, are at high risk for delivering before term. At this time, we do not have sufficient evidence to use any medication to help prevent these women from delivering early. Recently, preliminary studies have shown that progesterone may help prevent some women at high risk for preterm delivery from delivering early. Our study will investigate whether progesterone can help this specific group of women, women with arrested preterm labor, deliver healthy infants at term.

Detailed Description

The purpose of this study is to test the efficacy of progesterone in prolonging human pregnancies complicated by arrested preterm labor. Animal labor has not been shown to be equivalent to human labor and would not be an appropriate substitute for this study. In addition, this medication has been previously used in pregnant women without any evidence of significant harm to the mother or fetus. Women will be approached for enrollment in the study during their hospitalization for preterm labor. If they choose to enroll, they will have weekly MD visits at the obstetrical clinic, daily use of vaginal progesterone that will be self administered, and routine obstetric care at the time of recurrent labor and delivery. The daily progesterone is not a part of routine care for these patients. In addition, we will ask patients to fill out a written questionaire one week after starting the medication to describe any subjective symptoms that may be associated with this medication. Finally, we will assess the peripheral levels of progesterone with a blood draw prior to starting the mediation, one week after starting the medication, and at the time of recurrent pre-term labor or delivery. The first two of these blood draws will be in addition to the standard treatment. The final blood draw will involve collecting an extra sample at a time when the participant would normally have blood drawn as a part of routine care.

Registry
clinicaltrials.gov
Start Date
October 2009
End Date
March 2015
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Deirdre Judith Lyell

Associate Professor

Stanford University

Eligibility Criteria

Inclusion Criteria

  • Pregnant women with arrested preterm labor between 24+0 to 33+6 weeks pregnant.
  • Intact membranes
  • Singleton pregnancy
  • Greater than or equal to 18 years of age
  • Cervical dilation less than or equal to 4cm

Exclusion Criteria

  • Any contraindication to on-going pregnancy
  • Placental abruption
  • Placenta previa
  • Lethal fetal anomalies
  • Premature rupture of membranes
  • Multiple gestation
  • Less than 18 years old
  • Known allergy to any component of the study medication or placebo
  • Severe maternal medical illness

Arms & Interventions

Progesterone

Progesterone 400mg per vagina qhs.

Intervention: Progesterone

Polyethylene glycol&hydrogenated vegetable oil

Polyethylene glycol\&hydrogenated vegetable oil per vagina

Intervention: Polyethylene glycol&hydrogenated vegetable oil.

Outcomes

Primary Outcomes

Reduction in Delivery Rate Prior to 37 Weeks Gestation

Time Frame: Up to 37 weeks of gestation

Reduction in delivery rate prior to 37 weeks gestation (preterm birth).

Secondary Outcomes

  • Maternal Chorioamnionitis(Up to maternal hospital discharge)
  • Maternal Anticipated Adverse Medication Reaction(Up to the maternal discharge from delivery hospitalization)
  • Birthweight(At the time of newborn birth)
  • Neonatal Intensive Care Unit (NICU) Admission(At time of neonatal discharge)
  • Neonatal Morbidity(Up to 28 days after neonatal birth)
  • Neonatal Mortality(Up to 28 days after neonatal birth)
  • Neonatal Congenital Abnormalities(Up to the time of neonatal discharge from the delivery hospital)
  • Number of Days Delay of Delivery(Up to the time of delivery)

Study Sites (1)

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