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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorOctober 6 University

About this trial

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.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Patients aged 18-65 years.

Endodontically treated teeth requiring intra-radicular attachments.

Adequate oral hygiene .

Periodontally Compromised Teeth: When some teeth have reduced bone support but can still be maintained as overdenture abutments with proper treatment.

Disqualifiers

Severely Compromised Remaining Teeth: If the remaining teeth have poor prognosis due to extensive decay or severe periodontal disease.

Severe Bone Loss Around Abutment Teeth: If the remaining teeth do not provide adequate support, they may fail early, leading to additional complications.

Severe Malocclusion: Where occlusal discrepancies make overdenture placement difficult.

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.

Trial design

Design model

Crossover

Treatments tested in this trial

  • 3 shape desktop scanner

    Device

    Scanning of intra-radicular impression by desktop scanner

  • SHINING 3D intraoral scanner

    Device

    Direct scanning of the intra-radicular canal by Intraoral scanner A

  • Planmeca Emerald S intraoral scanner

    Device

    Direct scanning of the intra-radicular canal by Intraoral scanner B

Treatment groups

60 Participants
are divided into 3 treatment groups
Group A: Group IActive comparator 1 intervention
Group B: Group IIExperimental treatment 1 intervention
Group C: Group IIIExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Accuracy

measure accuracy between the dimension of the prepared canal gained by intra-radicular impression and the dimension of the prepared canal directly by two different types of intraoral scanners

Time frame
Immediately after scanning.

Secondary outcomes

1

Patient-reported comfort

Patient-reported comfort (assessed via a Likert scale questionnaire) Scaled from 0-100 The highest score means excellent The lowest score means unsatisfactory

Time frame
Immediately after impression taking and scanning.

Other outcomes

Sponsors and contacts

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