Comparison of influence of microgrooved grip and spiral implant with microgrooved abutment on peri-implant hard and soft tissues in A clinical trial
Not Applicable
- Conditions
- Health Condition 1: K068- Other specified disorders of gingiva and edentulous alveolar ridge
- Registration Number
- CTRI/2022/09/045655
- Lead Sponsor
- Dr Shreya Warkad
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Systemically healthy patient of at least 18 years of age
Partially edentulous requiring dental implants in the posterior region of the maxilla or mandible
Adequate volume of native or grafted bone to accommodate dental implants
Sites at which minimum torque of 35 Ncm is obtained at the time of implant insertion
Exclusion Criteria
General contraindications to implant surgery
Subjected to irradiation in the head and neck area within the last 6 months
Treated or under treatment with intravenous amino-bisphosphonates
Smokers or patients with poor oral hygiene
Patients with para-functional habits
Pregnant or lactating females
An acute or chronic infection at the site intended for implant placement
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate and compare peri-implant bone level between microgrooved grip implant and spiral implant with microgrooved abutment <br/ ><br> <br/ ><br>To evaluate and compare peri-implant soft tissues between microgrooved grip implant and spiral implant with microgrooved abutmentTimepoint: At baseline <br/ ><br>3 months <br/ ><br>6 months
- Secondary Outcome Measures
Name Time Method To evaluate bleeding on probing probing depth around implants restored with microgrooved grip implant with microgrooved abutment <br/ ><br> <br/ ><br>To evaluate bleeding on probing and probing depth around implants restored with spiral implant with microgrooved abutment <br/ ><br> <br/ ><br>To compare bleeding on probing and probing depth around implants restored with microgrooved grip implant and spiral implant with microgrooved abutment at baseline and 6 months post surgery <br/ ><br> <br/ ><br>To assess Peri-implant soft tissues with Testori Esthetic Score <br/ ><br> <br/ ><br>To assess patients satisfaction using VAS scaleTimepoint: At baseline <br/ ><br>3 months <br/ ><br>6 months