Bone density around implants by cone beam computed tomography
Not Applicable
- Conditions
- Health Condition 1: - Health Condition 2: null- Partially EdentulousHealth Condition 3: R00-R99- Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified
- Registration Number
- CTRI/2018/09/015776
- Lead Sponsor
- Divya Kadali
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients with partially edentulous sites were selected with age group between 20 to 50 years with good systemic health will be enrolled in the study
Exclusion Criteria
Any systemic disease that affect the periodontium and contraindicate for periodontal surgery
Patients with psychiatric disorders
Inability or unwillingness to complete the trial
Patients on medication
Poor oral hygiene
Pregnant lactating mothers
Smoking
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome was to evaluate Bone Mineral Density(BMD) by Hounsfield Units (HU) and Trabecular Bone microstructure by Fractal Dimension (FD) analysis around dental implants pre operatively and post operatively by Cone Beam Computed Tomography(CBCT).Timepoint: 0 to 6 months
- Secondary Outcome Measures
Name Time Method The secondary outcome was to evaluate Bone Mineral Density(BMD) by Hounsfield Units (HU) and Trabecular Bone microstructure by Fractal Dimension (FD) analysis around dental implants pre operatively and post operatively by Cone Beam Computed Tomography(CBCT).Timepoint: 0 to 6 months