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Clinical Trial Summary

The purpose of this study is to examine the effectiveness of the DynaCleft® system on soft tissues of infants with unilateral incomplete cleft lip and to assess influences on quality of life for infants who underwent DynaCleft® and that of their families.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04455035
Study type Interventional
Source The University of Texas Health Science Center, Houston
Contact Ahn Tran, DDS
Phone (713) 486-4150
Email Anh.T.Tran@uth.tmc.edu
Status Recruiting
Phase N/A
Start date September 21, 2020
Completion date June 1, 2021

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