Oral Progesterone for Prevention of Preterm Birth

Status Completed

Clinical Trial Summary

To evaluate whether daily oral micronized progesterone is effective in preventing recurrent spontaneous preterm birth (RSPB) and whether micronized progesterone use increases maternal serum progesterone levels.

Clinical Trial Description

To evaluate whether 400 mg daily oral micronized progesterone from 16 to 34 weeks' is effective in preventing recurrent spontaneous preterm birth (RSPB) and whether micronized progesterone use increases maternal serum progesterone levels. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01180296
Study type	Interventional
Source	Fetal Medicine Foundation
Contact
Status	Completed
Phase	Phase 3
Start date	November 2006
Completion date	January 2009

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