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Clinical Trial Summary

This randomized clinical trial (RCT) study investigates if there is any difference in complication rate between perforated dense-polytetrafluroethylene (d-PTFE) mesh vs perforated d-PTFE mesh covered with a native collagen membrane. The primary endpoint is complication rate. The secondary endpoints are regeneration rate and pseudoperiosteum formation.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04843488
Study type Interventional
Source Urban Regeneration Institute
Contact
Status Completed
Phase N/A
Start date January 1, 2021
Completion date May 2, 2023

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