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A comparative evaluation of prosthetic and biological outcome of two different implant restorative materials

Not Applicable
Conditions
Health Condition 1: K055- Other periodontal diseases
Registration Number
CTRI/2022/02/039915
Lead Sponsor
Taniya Malhotra
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1.Two implants placed in the same arch in posterior quadrant requiring prosthodontic rehabilitation.

2.Interocclusal restorative space of 8-10 mm

3.Healthy Periodontium with no visible signs of bruxism

4.Stable and healthy implants with no crestal bone loss

Exclusion Criteria

1. According to ASA Classification Class 4 patients:

Organic heart disease with marked signs of cardiac insufficiency

Recent myocardial infarction of less than 6 months duration.

Unstable angina.

Patients with advanced degrees of pulmonary, renal or endocrine insufficiency

2. According to ASA Classification Class 3 patients

Diabetes with complications to vascular or other organs, i.e., retinopathy, neuropathy, etc.

3. Occlusal anomalies

Deep Bite

Cross Bite

4. Long term edentulism leading to mesial drifting of adjacent teeth or supraaeruption of opposing teeth

5.Para-functional Habits (Bruxism)

6.Smokers

7.Active periodontal disease

8.Allergy to materials used in the study

9.Current drug abuse

10.Pregnant or intend to become pregnant.

11.Severe salivary gland dysfunction.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
primary outcome will determine which restoration will be more suitable for implant supported prosthesis. <br/ ><br>The suitabilty of the restorations will depend on the prosthetic and biologic outcome which will include ceramic fracture, screw loosening, marginal fit, color match, occlusal wear, bleeding on probing, plaque deposition etcTimepoint: primary outcome will determined at baseline, 6 months and 12 months
Secondary Outcome Measures
NameTimeMethod
To Determine the biological outcome through evaluation of inflammatory markers of two different implant restorative materials. The inflammatory marker to be evaluated is MMP-8.Timepoint: Biological outcome will be assessed at baseline, 6 months and 12 months
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