Evaluating the effect of ossseodensification technique of implant placement on bone around dental implants.
Not Applicable
- Conditions
- Health Condition 1: K084- Partial loss of teeth
- Registration Number
- CTRI/2023/03/050409
- Lead Sponsor
- Husbana Bakrolwala
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Age group 18 and above and patient willing to participate in the study.
2.Patients with edentulous space in the maxillary jaw having healed bone site indicated for rehabilitation with implants.
3.Patient having sufficient residual bone volume for implant placement.
4.Patient having good general health with no systemic disease.
5.Patient having adequate oral hygiene.
Exclusion Criteria
1.Patients with para functional habits such as bruxism and clenching.
2.Patients with local limitations such as inadequate inter-ridge distance.
3.Patients who consume alcohol, smoke or use illicit drugs.
4.Patient with any systemic disease, irradiated patients, patients with previous or active treatments with steroids or bisphosphonates
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To analyse and compare levels of BMP-9 in peri-implant crevicular fluid (PICF) around implants placed using osseodensification (OD) drilling protocol and conventional drilling protocol.Timepoint: 2 weeks, 8 weeks, 16 weeks
- Secondary Outcome Measures
Name Time Method To compare primary and secondary stability of implants placed using Osseodensification drilling protocol and Conventional drilling protocol.Timepoint: At the time of implant placement, 2 weeks, 8 weeks;To compare the crestal bone loss around implants placed using Osseodensification drilling protocol and Conventional drilling protocol.Timepoint: Baseline, 2 weeks, 8 weeks, 16 weeks, 6 months