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Clinical Trial Summary

The purpose of this study is to determine the effectiveness of buccal misoprostol and comparing this with vaginal route of the same drug.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Pharmacokinetics/Dynamics Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00892229
Study type Interventional
Source Hawler Medical University
Contact
Status Completed
Phase Phase 2
Start date March 2007
Completion date March 2008

See also
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