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Deviation Parameters of Intraorfal Scanning in Capturing Different Intraoral Defects

Cairo University (CU) logo

Cairo University (CU)

Status

Completed

Conditions

Nasal Defect

Treatments

Device: Scanning using intraoral scanner without markers
Device: Scanning using intraoral scanner with markers
Device: Physical Impression

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

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.

Enrollment

15 patients

Sex

All

Volunteers

Accepts Healthy Volunteers

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.

Trial design

Primary purpose

Other

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

15 participants in 3 patient groups

Physical impression
Active Comparator group
Treatment:
Device: Physical Impression
Scanning using intraoral scanner without markers
Experimental group
Treatment:
Device: Scanning using intraoral scanner without markers
Scanning using Intraoral scanner with markers
Experimental group
Treatment:
Device: Scanning using intraoral scanner with markers

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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