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Not yet recruiting Not applicable NCT07403851

Effect of Scanning Technology on the Accuracy of Digitally Customized Intraradicular Attachments

No applicable phase (e.g. observational)
Conditions: Scanning Devices

Sponsor: October 6 University

trial.available_in: БГ
Overview
This study aims to evaluate the accuracy of intra-radicular attachments fabricated by direct scanning using three different scanners in vivo. The primary outcome will be the accuracy of the fabricated attachments, while secondary outcomes will includepatient-reported comfort during procedure of taking intraradicular attachment conventional impression and direct scanning.
Description
The fabrication of intra-radicular attachments is a critical step in restoring endodontically treated teeth. The accuracy of these restorations directly impacts their clinical performance, including retention, marginal fit, and long-term success. With advancements in digital dentistry, intraoral scanners (IOS) have become increasingly popular for direct scanning of intra-radicular preparations. However, the accuracy of these scanners varies depending on their technology, software, and clinical conditions
Who can participate
Inclusion Criteria: 1. Patients aged 18-65 years. 2. Endodontically treated teeth requiring intra-radicular attachments. 3. Adequate oral hygiene . 4. Periodontally Compromised Teeth: When some teeth have reduced bone support but can still be maintained as overdenture abutments with proper treatment. Exclusion Criteria: 1. Severely Compromised Remaining Teeth: If the remaining teeth have poor prognosis due to extensive decay or severe periodontal disease. 2. Severe Bone Loss Around Abutment Teeth: If the remaining teeth do not provide adequate support, they may fail early, leading to additional complications. 3. Severe Malocclusion: Where occlusal discrepancies make overdenture placement difficult. 4. Limited inter-arch Space: cann't accommodate the overdenture components. 5 . Poor Oral Hygiene: increase the risk of decay or periodontal issues in retained abutments.
Interventions
3 shape desktop scanner
DEVICE
SHINING 3D intraoral scanner
DEVICE
Planmeca Emerald S intraoral scanner
DEVICE
Locations

Location information is not available.

Technical details
Status
Not yet recruiting
Phase
Not applicable
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Maximum age
65 Years
Healthy volunteers
No
Start date
01.05.2026
Completion date
01.08.2026
Registry ID
NCT07403851
Source
clinicaltrials.gov
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