Nasal Defect Clinical Trial
Official title:
Accuracy of Conventional Impression Versus Intraoral Scanner in Capturing Three Different Nasal Defects With and Without Skin Markers
Verified date | March 2024 |
Source | Cairo University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
Status | Completed |
Enrollment | 15 |
Est. completion date | February 20, 2024 |
Est. primary completion date | February 20, 2024 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | N/A and older |
Eligibility | Inclusion Criteria: - isolated nasal defects either, total or subtotal. - congenitally missing external nose with healthy and intact remaining facial structures. Exclusion Criteria: - Any debilitating medical condition. |
Country | Name | City | State |
---|---|---|---|
Egypt | Cairo University | Cairo |
Lead Sponsor | Collaborator |
---|---|
Cairo University |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Dimensional accuracy of intraoral scanners | measuring dimensional accuracy of diffrent scanning techniques using intraoral scanners | Day 0 |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
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