A study using fibrinogen obtained by spinning patients own blood to coat the surface of implant to be placed in order to achieve faster bonding between bone and implant.
Not Applicable
- Conditions
- Health Condition 1: Z768- Persons encountering health services in other specified circumstances
- Registration Number
- CTRI/2020/08/027288
- Lead Sponsor
- Vijyanta Suman
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1) single or multiple missing teeth in patients
2) Age group from 22-50 years
3) Non smokers
4) Patients with no bone diseases.
Exclusion Criteria
1) Patients with debilitating systemic diseases
2) Patients with inadequate interocclusal clearance
3) Patients with inadequate mesio-distal space in the edentulous area
4) Patients on medications known to interfere with wound and bone healing
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary Implant stabilityTimepoint: 1 month and 3 months
- Secondary Outcome Measures
Name Time Method not applicableTimepoint: not applicable