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The aim of this study is to evaluate clinically and radiographically soft tissue around single-implant crowns and peri-implant bone resorption respectively by using zirconia implants or titanium implants in horizontally deficient partially edentulous ridges.
Full description
Experimental: Main treatment group Zirconia implants will be placed in a prosthetically guided position in horizontally deficient ridges in main treatment group.
Active Comparator: Control group Titanium implants will be placed in a prosthetically guided position in horizontally deficient ridges in control group.
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Inclusion and exclusion criteria
Inclusion Criteria: Based on the classification of alveolar ridge width given by Tolstunov, subjects with
Exclusion Criteria:
Medically compromised patients
-. Subjects who underwent radiotherapy or chemotherapy and with
Habit of smoking, tobacco and alcohol abuse
Subjects with active periodontal disease to residual dentition and lack of oral hygiene will be excluded from this study.
Primary purpose
Allocation
Interventional model
Masking
24 participants in 2 patient groups
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Central trial contact
R V Chandra, MDS;DNB;PhD
Data sourced from clinicaltrials.gov
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