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Evaluation of wear of natural tooth opposing crowns of different materials

Phase 3
Registration Number
CTRI/2024/03/064627
Lead Sponsor
Dr Shivani Anand
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

a)Subjects needing a crown on either 2nd Premolar or 1st molar of any arch.

b)Subjects having normal Class I Angle’s occlusion.

c)Presence of natural antagonist against the proposed full coverage restoration.

d)Presence of same tooth on the contralateral side with natural antagonist for comparative analysis.

e)Subjects with similar facial biotype.

Exclusion Criteria

a)Subjects with parafunctional habits, for example bruxism.

b)Subjects with temporomandibular joint disorder and habit of unilateral mastication.

c)Subjects likely to shift out of the area within the 6 months duration of the study.

d)Subjects with excessive wear of posterior teeth i.e. dentinal exposure.

e)Subjects with restored antagonist tooth opposing the test group tooth or the contralateral side tooth.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
)To evaluate the wear of natural enamel antagonist to -: <br/ ><br>I)Monolithic lithium disilicate crown <br/ ><br>II)Monolithic zirconia crowns <br/ ><br>III)PEEK coping layered with lithium disilicate crowns <br/ ><br>Timepoint: baseline, 9 months
Secondary Outcome Measures
NameTimeMethod
To compare wear of natural enamel antagonist to above restorative crowns with enamel to enamel wear on contralateral side in same pair of opposing teeth.Timepoint: baseline, 9 months
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