Evaluation of new iranian implant system
Not Applicable
- Conditions
- Edentolous.Loss of teeth due to accident, extraction or local periodontal disease
- Registration Number
- IRCT20151017024573N5
- Lead Sponsor
- Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
Short 3 unit bridge or single edentolous
1 mm bone around implant
Exclusion Criteria
Augmentation in implant site
Infection in implant site
Smokers
uncontrolled dibetic patients or any disorders that affect treatment results
Bisphosphonate intake
Active periodontal disease
bruxism or clenching
Pregnancy
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Bleeding on probing. Timepoint: 6 and 12 month after implant insertion. Method of measurement: probe.;Bone level at mesial and distal of implant. Timepoint: immediately after surgery and 6 and 12 month later. Method of measurement: periapical radiography.;Pocket depth. Timepoint: 6 and 12 month after implant placement. Method of measurement: probe.
- Secondary Outcome Measures
Name Time Method