comparing efficacy of two implants
Not Applicable
- Conditions
- Health Condition 1: K084- Partial loss of teeth
- Registration Number
- CTRI/2022/01/039353
- Lead Sponsor
- Translational Center of Excellence on Biomaterials for Orthopedic and Dental Applications
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Absence of mandibular first molar unilaterally
Bounded edentulous space with natural teeth with minimum period of 4 months after extraction
More than 2 mm thickness of keratinised tissue around planned edentulous site
Presence of opposing natural dentition with normal occlusion
Presence of adequate bone around implant and vital structure
Good to fair oral hygiene
Exclusion Criteria
No systemic disease
Presence of any local risk factor like insufficient crown space or infected site
History of smoking
Bruxism and other parafunctional oral habits
Lactating and pregnant women
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method mean crestal bone loss <br/ ><br>Timepoint: Baseline, 4 and 12 months
- Secondary Outcome Measures
Name Time Method ongevity of restoration and technical complication <br/ ><br> <br/ ><br>Marginal bone loss and probing depth of soft tissue <br/ ><br> <br/ ><br>Cone beam computed tomography (CBCT) analysis to quantify hard tissue stability or loss around the crest of the coated implant <br/ ><br> <br/ ><br>Dental implant stability by using Resonance frequency analyserTimepoint: Four and twelve months