Measuring primary stability and peri implant bone density using osseodensification protocol
Phase 1
- Registration Number
- CTRI/2019/03/018046
- Lead Sponsor
- Vishal Alampur
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
patients with single and multiple edentulous maxillary sites which require indirect sinus lift
Exclusion Criteria
Pregnant women, lactating mother, patients allergic to pencillin, cephalosporins, local anaesthetic drugs, analgesics and anti inflammatory drugs. Patients who are smokers
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method to compare osseodensification protocol with conventional implant protocolTimepoint: Baseline and 3 months
- Secondary Outcome Measures
Name Time Method to compare osseodensification protocol with conventional implant protocolTimepoint: At baseline and 3 months