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Clinical Trial Summary

Pharmacokinetic analysis of 200mg vaginal progesterone suppository in women with singleton pregnancies between 18 0/7- 23 6/7 weeks' gestation


Clinical Trial Description

Prospective study of 6 women with singleton pregnancies 18 0/7- 23 6/7 weeks' gestation with no prior preterm birth or short cervix who are administered a single dose of 200mg vaginal progesterone suppository. Serum progesterone levels will be drawn serially from pre-dose to 24 hours post-dose. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03340701
Study type Interventional
Source Thomas Jefferson University
Contact
Status Completed
Phase Phase 1
Start date November 6, 2017
Completion date June 30, 2018

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