Assessment of The Accuracy of Complete Crown 3D Superimposition Technique Relative to The Gold Standard Technique for Digital Quantification of Volumetric Soft Tissue Changes in The Esthetic Zone

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-60
SponsorBritish University In Egypt

About this trial

The aim of this study is to assess the precision of the complete crown technique employed for the superimposition of 3D models, specifically in the quantitative volumetric evaluation of gingival tissues. This technique was initially introduced in an in-vitro study by Dritsas et al. (2023) as a means to achieve an accurate, reproducible, and simple method for quantification of gingival recession.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Patients aged 18 years or older.

Patients requiring esthetic crown lengthening.

Full-mouth plaque and bleeding score not exceeding 20%.

Presence of at least 2.5 mm keratinized tissue width (Pontoriero & Carnevale, 2001).

Disqualifiers

Systemic health conditions that contraindicate or affect healing of periodontal surgery.

Patients requiring prosthetic crowns or restorations in the esthetic zone.

Gummy smile with normal tooth proportions.

Patients treated with medications known to affect the gingiva (Phenytoin, Cyclosporine and Nifedipine).

Trial design

Design model

Single group

Treatments tested in this trial

  • Group I

    Diagnostic test

    Complete Crown technique of superimposition

  • Group II

    Diagnostic test

    Gold standard technique of superimposition

Treatment groups

12 Participants
are divided into 1 treatment group
Group A: group IExperimental treatment 2 interventions

Trial outcomes

Primary outcomes

1

Superimposition accuracy

Using Geomagic Software (RMS) in Millimeter(mm)

Time frame
6 months

Secondary outcomes

1

Soft tissue volumetric Changes

Digital using intraoral scanner and blenderfordental software in Millimeter(mm)

Time frame
6 months
2

Gingival Margin level change

Digital using intraoral scanner and blenderfordental software in Millimeter(mm)

Time frame
6 months
3

Intra-Inter Assessor reliability

Intraclass correlation coefficient

Time frame
6 months
4

Operator's satisfaction

Questionnaire

Time frame
6 months

Other outcomes

Sponsors and contacts

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British University In Egypt

Lead sponsor

Cairo University

Collaborator

This trial is not recruiting at the moment. You can still explore other options: