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Deviation Parameters of Intraorfal Scanning in Capturing Different Intraoral Defects

NCT06315621 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 15

Last updated 2024-09-05

No results posted yet for this study

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.

Conditions

  • Nasal Defect

Interventions

DEVICE

Scanning using intraoral scanner with markers

Scanning different types of nasal defects using intraoral scanner with skin markers.

DEVICE

Scanning using intraoral scanner without markers

Scanning different types of nasal defects using intraoral scanner without skin markers.

DEVICE

Physical Impression

Recording different types of nasal defects using physical impressions

Sponsors & Collaborators

  • Cairo University

    lead OTHER

Study Design

Allocation
NON_RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-02-01
Primary Completion
2024-02-20
Completion
2024-02-20

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06315621 on ClinicalTrials.gov