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NCT00579553 · ClinicalTrials.gov registry record · NA
Comparing IM vs. Vaginal Progesterone for Pre-term Birth
A NA study, sponsored by University of Oklahoma.
- Completed
- Registry status
- NA
- Development phase
- 174
- Enrollment target
NCT00579553 is a NA study that has completed, run by University of Oklahoma. The registered enrollment target is 174 participants.
The verdict
NCT00579553, a NA study, has completed, sponsored by University of Oklahoma.
- COMPLETED
- Registry status
- NA
- Development phase
- 174 participants
- Enrollment target
Study 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.
Interventions
- DRUG Vaginal Progesterone
- DRUG Intramuscular Progesterone
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 174 participants |
| Start Date | 2006-10 |
| Est. Completion | 2011-05 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00579553
The ClinicalTrials.gov registry entry for NCT00579553 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 174 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Oklahoma, which has 358 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Vaginal Progesterone is the first listed.
NCT00579553 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00579553 about?
NCT00579553 is a clinical study titled "Comparing IM vs. Vaginal Progesterone for Pre-term Birth". 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 t...
What is the current status of trial NCT00579553?
This trial is currently completed. It is a NA study. The enrollment target is 174 participants. The study started on 2006-10. Estimated completion is 2011-05.
What interventions are being tested in trial NCT00579553?
The interventions under investigation include: Vaginal Progesterone (DRUG), Intramuscular Progesterone (DRUG).
Who is sponsoring clinical trial NCT00579553?
This trial is sponsored by University of Oklahoma, which has 358 total clinical trials registered on ClinicalTrials.gov.
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