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Clinical Trial Summary

The purpose of this investigation is to assess the use of a novel scaffold (an FDA-approved collagen-hydroxyapatite material called Syn-Oss) for regeneration of pulp tissues versus the use of a traditional scaffold (blood clot).


Clinical Trial Description

Regeneration of pulp tissues in teeth with immature roots is a new concept based on historical limited success using calcium hydroxide dressings placed into debrided pulp spaces. Obtaining stem cells from the apical papilla (SCAP cells), which are present at the base of all teeth, but are most accessible in teeth with immature apices, greatly enhances clinical success. Current therapies lack ideal messenger chemicals and scaffolds to optimize results. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03613090
Study type Interventional
Source University of Alabama at Birmingham
Contact
Status Withdrawn
Phase Phase 2
Start date April 1, 2019
Completion date April 1, 2019

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