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Clinical Trial Summary

For all participants, a conventional facial impression will be done using silicone material then poured and scanned using a desktop scanner which represented the control group (Group 1). Group 2, involves nasal defects which will be optically scanned using IOS(medit 700 wireless) without facial markers Group 3 involves nasal defects which will be optically scanned using IOS(medit 700 wireless) with facial markers. STL files of the facial scans and scanned cast obtained from the impression will be exported and saved to be used later for outcome assessment.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06315621
Study type Interventional
Source Cairo University
Contact
Status Completed
Phase N/A
Start date February 1, 2024
Completion date February 20, 2024

See also
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