Peri-implant tissue response to PEEK and Titanium implant abutments: An In-vivo Six Months Randomized Controlled Clinical Study.
- Registration Number
- CTRI/2019/06/019545
- Lead Sponsor
- Manika Mittel
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Closed to Recruitment of Participants
- Sex
- Not specified
- Target Recruitment
- 0
Subjects having good systemic health and mental condition maintaining optimum oral hygiene care, with the presence of adequate bone volume and inter-arch space to accommodate implant prosthesis of appropriate size, with stable occlusal relationship and available for 1 year of investigations were included in the study.
Exclusion criteria were: Subjects having systemic diseases (diabetes mellitus, rheumatoid arthritis, cardiovascular diseases, etc.) that would preclude surgical procedure, physical and mental disabilities that would conflict with the capability to perform adequate oral hygiene, pregnant and lactating mothers; insufficient bone volume requiring augmentation of the implant site; active infection or severe inflammation in the areas intended for implant placement; subjects currently receiving intravenous or oral bisphosphonate therapy; subjects with severe bruxism or clenching habits; treatment with therapeutic radiation to the head region within the past 12 months; alcohol or drug abuse and smoking
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Clinical evaluation of peri-implant soft and hard tissue parameters, radiological and biochemical examinations of the reconstructions will be performed immediately after crown insertion baseline, at 12 weeks and at 24 weeks of function.Timepoint: Clinical evaluation of peri-implant soft and hard tissue parameters, radiological and biochemical examinations of the reconstructions will be performed immediately after crown insertion baseline, at 12 weeks and at 24 weeks of function.
- Secondary Outcome Measures
Name Time Method Clinical evaluation of peri-implant soft and hard tissue parameters, radiological and biochemical examinations of the reconstructions will be performed immediately after crown insertion baseline, at 12 weeks and at 24 weeks of function.Timepoint: Clinical evaluation of peri-implant soft and hard tissue parameters, radiological and biochemical examinations of the reconstructions will be performed immediately after crown insertion baseline, at 12 weeks and at 24 weeks of function.