Clinical Trials Directory

Trials / Completed

CompletedNCT00579553

Comparing IM vs. Vaginal Progesterone for Pre-term Birth

Comparing Intramuscular Versus Vaginal Progesterone for Prevention of Preterm Birth.

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
174 (actual)
Sponsor
University of Oklahoma · Academic / Other
Sex
Female
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

This is a randomized controlled trial comparing weekly intramuscular injection of 17 alpha hydroxylprogesterone caproate with daily vaginal progesterone in women with singleton pregnancies and history of prior spontaneous preterm birth in terms of maternal, fetal and neonatal outcomes. Our aim is to assess the effects on maternal, fetal and neonatal outcomes of antenatal progesterone administered intramuscularly versus vaginally in women with singleton pregnancy and a history of prior preterm birth.

Detailed description

This study is intended as a randomized controlled trial. Women with singleton pregnancies between 16 and 20 weeks 6 day will be randomized to one of two treatment groups. Those randomized to weekly intramuscular progesterone will receive 250 mg of 17 alpha hydroxyprogesterone caproate every week in the clinic between randomization and delivery for those delivery preterm or 36 weeks 6 days. While those randomized to vaginal progesterone will receive 100 mg vaginal progesterone daily at home. Vaginal progesterone to last between clinic visits will be provided to subject. Those women in the vaginal progesterone group will also be informed on how to obtain additional medication in case of missed clinic appointment. Treatment will be continued until 36 weeks 6 days or as dictated by date of preterm delivery.

Conditions

Interventions

TypeNameDescription
DRUGIntramuscular ProgesteroneIntramuscular Progestone: 17 alpha hydroxyprogesterone caproate: weekly 1 cc injections containing 250 mg of 17P
DRUGVaginal ProgesteroneVaginal Progesterone: 100 mg vaginal suppository daily

Timeline

Start date
2006-10-01
Primary completion
2011-05-01
Completion
2011-05-01
First posted
2007-12-24
Last updated
2021-05-19
Results posted
2021-05-19

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00579553. Inclusion in this directory is not an endorsement.