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Clinical Trial Summary

This is a prospective, open, non-comparative and baseline-controlled study to evaluate efficacy and safety of Macrolane VRF20 treatment in 40 subjects with pectus excavatum deformity. Each subject participating in the study will be treated with approximately 50-150 ml of Macrolane VRF20. The amount of study product used will be individually determined in order to achieve an optimal correction of the deformity in each subject.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01750112
Study type Interventional
Source Galderma R&D
Contact
Status Completed
Phase N/A
Start date December 2012
Completion date September 2016