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Clinical and Radiographical Evaluation of CAD-CAM Crowns With and Without Deep Margin Elevation

Clinical and Radiographical Evaluation of CAD-CAM Crowns With and Without Deep Margin Elevation: Up to 10-year Results

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06114030
Enrollment
560
Registered
2023-11-02
Start date
2023-03-01
Completion date
2024-01-30
Last updated
2023-11-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Broken Teeth, Caries,Dental, Crown of Tooth With Poor Contour, Failure, Prosthesis, Survival, Prosthesis

Brief summary

Deep margin elevation (DME) is a non-invasive restorative technique to relocate the deep cervical margin to a supragingival position using resin composite. This retrospective multicenter practice-based study will assess the long-term clinical performance and periodontal health of teeth restored with CAD-CAM crowns with or without DME. Patients who will receive CAD-CAM lithium disilicate (LD) crowns with or without DME between 2013 and 2023 at multiple private practices will be included. When indicated, DME will be performed using resin-based restoration. Clinical assessment of the crowns and supporting periodontal structures will be performed following the modified United States Public Health Service (USPHS) criteria. Intra-oral photographs, periapical and bitewing radiographs will be taken for further assessment by three evaluators. Kaplan Meier survival analyses will be performed.

Detailed description

The ethical approval to conduct this retrospective multicenter practice-based study was obtained from the Research Ethics Committee at the University of Sharjah (REC-23-09-11-01-F). The present report will complie with the STROBE guidelines for cohort studies. Participants selection Patient records at 7 private practices in the UAE will be searched for the presence of posterior LD CAD-CAM crowns during 2013 to 2016. Inclusion criteria: adult patient and indication for crown with or without DME. Exclusion criteria: poor oral hygiene and active periodontal disease. A total of 560 eligible patients will be invited to a clinical examination. Clinical Examination The clinical evaluation will be conducted by three calibrated independent prosthodontists. Patients will be requested to read and sign an informed consent form to participate in the study. Intraoral photographs, Periapical and bitewing radiographs will be obtained to assess the emergence profile of the DEM which should ideally reproduce the normal morphology. Both the crowned tooth and the contralateral tooth were assessed clinically for the following parameters: pocket depth (PD), BoP, and presence of plaque using a plaque indicator liquid (Mira-2 Ton Liquid, Hager & Werken; Duisburg, Germany). Bone level will be assessed by comparing a measurement from the margin of the tooth to the crest of the bone on bitewing radiographs to corresponding preoperative radiographs. A comprehensive assessment of the restored teeth will be carried out following the modified United States Public Health Service (USPHS) criteria. The location of crown margin will be recorded clinically and radiographically to assess the association between periodontal health and margin location. The primary outcomes will be the survival rate and time to event. The secondary outcome will be the success rate. The success is defined as a crown that had remained unchanged over the observation period, while survival is defined as a crown that was in situ at the examination visit but might exhibits chipping or have been repaired. Failure will be scored for the followings: recurrent caries, loss of vitality, tooth fracture, and crown fracture. Statistical analysis Descriptive statistics were computed with a statistical software program (IBM SPSS Statistics, v29; IBM Corp., Armonk, NY, USA). Each complication will be considered as a statistical event. The statistical testing will be 2-tailed (a=.05). The McNemar chi-squared and Fisher exact tests will be used to assess the severity of PD, BoP and plaque deposition. Odds ratios and their 95% confidence intervals will be reported. The Pearson chi-squared test for differences in proportions will be used to assess the relationship between the location of margins and the associated condition of the periodontal tissues. Kaplan-Meier survival analysis will be performed to calculate the overall crown survival and success probabilities. Cox regression models will be used to evaluate the effect of various confounding factors on the survival and success rates.

Interventions

PROCEDUREDeep margin elevation with composite resin and Lithium disilicate glass-ceramic crowns

Restoration of the deep margin by composite restorations such as: Filtek Supreme XTE, Tetric EvoCeram, Estelite Sigma Qquick followed by Lithium disilicate glass-ceramic CAD/CAM crowns (IPS e.max CAD).

Sponsors

University of Sharjah
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

: * adult patient and indication for crown with or without DME.

Exclusion criteria

* poor oral hygiene and active periodontal disease.

Design outcomes

Primary

MeasureTime frameDescription
The survival rate of teeth restored with or without DME and crowns.10 yearsNumber of survived crowns in the presence or absence of DME
Number of failed crowns in the presence or absence of DME10 years

Secondary

MeasureTime frameDescription
Change from baseline in pocket depth10 years
Change from baseline in bleeding of probing10 years
Periodontal responses in response to deep (subgingival) margins10 yearsChange from baseline in bone level cervically

Countries

United Arab Emirates

Contacts

Primary ContactAhmed M Aziz, PhD
a.aziz@sharjah.ac.ae+97165057312
Backup ContactSama Suliman, MS
s.suliman@sharjah.ac.ae+9715057370

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026