Evaluation of effectivness of membrane made from human platelet concentrate with bioresorable ones using demineralised bone graft in treatment of periodontal defects
- Conditions
- Health Condition 1: K053- Chronic periodontitis
- Registration Number
- CTRI/2020/06/025979
- Lead Sponsor
- Dr Chitrika Subhadarsanee
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1)Presence of Class II furcation defect involving either buccal or lingual surfaces of the mandibular molars as determined by clinical and radiographic evaluation.
2)Presence of <= 3mm horizontal furcation probing depth.
3)Presence of <= 3mm of vertical furcation probing depth.
4)The experimental tooth should have proximal bone height coronal to the inter-radicular bone level.
5)Presence of sufficient amount of keratinized tissue.
6)The experimental tooth should have intact tooth surfaces adjacent to the furcation area and should have a normal response to the electric pulp test.
7)The gingival margin of the experimental tooth should be coronal to the furcation fornix.
8)Patients with no complicated medical history
9)Radiographic evidence of furcation defects in the molars (buccal ,lingual ,mesiobuccal or distobuccal).
1)Patients who are non-compliant to periodontal maintenance program
2)Patients who are smokers or use any other tobacco products.
3)Patients exhibiting tooth mobility for the selected tooth.
4)Confirmed allergy to the graft material, local anesthetics, chlorhexidine, antibiotics and analgesics .
5)Previous history of any periodontal regenerative therapy at the selected site.
6)Pregnant or lactating females.
7)Patients having infectious diseases such as hepatitis, HIV or tuberculosis.
8)Patients with previous systemic conditions and pregnant females.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method