A CLINICAL TRIAL TO STUDY THE EFFECT OF ALENDRONATE GEL IN CLASS II FURCATION DEFECT
Phase 4
- Conditions
- Health Condition 1: K088- Other specified disorders of teethand supporting structures
- Registration Number
- CTRI/2023/07/055485
- Lead Sponsor
- PRAVARA INSTITUTE OF MEDICAL SCIENCES, LONI
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1)Patient between age 30 â?? 50 years of either sex
2)Patient with bilateral mandibular class II furcation defect
3)Patient ready to give informed consent
4)Patients with endodontically vital tooth
5)Depth of furcation 2-4 mm
Exclusion Criteria
1)Patient with known systemic disease
2)Patient receiving systemic Alendronate sodium
3)Patient with known allergy to alendronate sodium
4)Pregnant lactating females
5)Use of tobacco in any form
6)Patient with unilateral class II furcation
7)Patients who have taken any type of periodontal therapy prior to 6 months of initial examination
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method effectiveness of alendronate gel under clinical parameters like probing depth and clinical attachment level along with bone fill of furcation defectTimepoint: 6 months
- Secondary Outcome Measures
Name Time Method effectiveness of alendronate under clinical <br/ ><br>parameters like probing depth & clinical <br/ ><br>attachment level along with bone fill of furcation <br/ ><br>defect in correlation to age & genderTimepoint: 3 months