A clinical trial to compare the effects of A-PRF and L-PRF in the treatment of intrabony periodontal defects
- Conditions
- Health Condition 1: K053- Chronic periodontitisHealth Condition 2: R50-R69- General symptoms and signs
- Registration Number
- CTRI/2020/11/028962
- Lead Sponsor
- ot applicable
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Two and three-wall intrabony defects greater or equal than 3 mm on an intraoral periapical radiograph [IOPA]along with a probing depth (PD) of greater or equal than 5 mm after Phase 1 therapy (scaling and root planning [SRP] in an asymptomatic tooth.
Age group -30-65years.
Absence of caries , pulpal pathology and severe occlusal interference at selected site.
Systemically healthy, non â??lactating, non-pregnant with no contraindication for periodontal surgery
Patients who give consent
Systemic illness known to affect the outcomes of periodontal therapy;
Individuals allergic to medications.
Pregnant or lactating women
Patients using tobacco in any form
Patients with unacceptable oral hygiene (PI greater than 1.5)
Patients with gingival recession, endodontic pulpal involvement ,or mobility of tooth greater than or equal to grade 2(15).
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Modifications to centrifugation speed and time with the low-speed concept is expected to produce <br/ ><br>Decrease in probing pocket depth <br/ ><br>Increase in clinical attachment level. <br/ ><br> <br/ ><br>Timepoint: 1 month <br/ ><br>
- Secondary Outcome Measures
Name Time Method Increase bone regeneration. <br/ ><br>Timepoint: 6 months