Clinical and radiographic evaluation and comparision of the effects of definitive abutment versus conventional repeated abutment disconnection and reconnection on peri-implant tissues.
Not Applicable
Completed
- Registration Number
- CTRI/2018/09/015726
- Lead Sponsor
- one
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 20
Inclusion Criteria
1.Systemically healthy patient of at least 21 years of age.
2.Partially edentulous maxilla or mandible requiring dental implant/s.
3.Adequate volume of native or grafted bone to accommodate dental implants.
4.Sites at which minimum torque of 35 Nm is obtained at the time of implant insertion.
Exclusion Criteria
1.General contraindications to implant surgery.
2.Individuals subjected to irradiation in the head and neck area, within the last 6 months.
3.Patients treated or under treatment with intravenous amino-bisphosphonates.
4.Smokers or patients with poor oral hygiene.
5.Patients with para-functional habits.
6.Pregnant or lactating females.
7.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 The primary outcome will be peri-implant marginal bone level measured from the implant shoulder to the crest of the bone at baseline and 6 months after loading, using RVG and CBCT.Timepoint: baseline and 6 months after loading
- Secondary Outcome Measures
Name Time Method The secondary outcome will be Plaque index, Bleeding on probing and Probing depth, measured at 3 and 6 months after implant insertion, by using UNC 15 probe. <br/ ><br>Patient satisfaction will be assessed by a questionnaire at baseline and 6 months.Timepoint: baseline, 3 months and 6 months.