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To compare the effect on surrounding structures by two different joints between artificial root and artificial tooth

Not Applicable
Completed
Conditions
Health Condition 1: K084- Partial loss of teeth
Registration Number
CTRI/2021/01/030194
Lead Sponsor
I
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
44
Inclusion Criteria

1. Patient in the age group of 18years or above who will be able to understand the procedure and be able to provide informed consent to participate in it.

2. Partially edentulous in posterior region(molar and premolar).

3. Patients with simplified oral hygiene index score less than 3

4. Patients having sufficient bone to allow optimal implant placement without the need of bone augmentation or recontouring and having sufficient distaance from vital tissues(2mm).

5. Presence of keratinized tissue more than 2mm

6. Stable posterior occlusion

7. Presence of adjacent teeth (1.5mm)

Exclusion Criteria

1. Patient with a history of systemic disease that precludes standard implant therapy.

2. Patients having parafunctional habits

3. Patient with a current daily smoking habit or chewing tobacco and with a history of drug abuse or alcoholism within past years

4. Pregnant or lactating mother

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
evels of Crestal bone loss <br/ ><br>Levels of IL-1beta <br/ ><br>Change in probing depth <br/ ><br>Change in bleeding on probing indexTimepoint: parameters will be recorded during the time of delivery of prosthesis <br/ ><br>3 months after occlusal loading <br/ ><br>6 months after occlusal loading <br/ ><br>12 months after occlusal loading
Secondary Outcome Measures
NameTimeMethod
ilTimepoint: Nil
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