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Clinical Trial Summary

The primary objective is the area of newly formed bone (%) as assessed by histomorphometry with either MD05 or beta-TCP.


Clinical Trial Description

n/a


Study Design

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


Related Conditions & MeSH terms


NCT number NCT00520377
Study type Interventional
Source Scil Technology GmbH
Contact
Status Active, not recruiting
Phase Phase 2
Start date January 2005
Completion date May 2008

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