To assess the combined effect of Virechana, Pratisarana and Gandoosha in Periodontitis.
Phase 3
- Conditions
- Health Condition 1: K053- Chronic periodontitis
- Registration Number
- CTRI/2022/01/039130
- Lead Sponsor
- Amrita School of Ayurveda
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients of age 20-60years
Chronicity less than 5years
Minimum of 3 sites with >=4mm pocket depth
Minimum of 3 sites that bleed on probing
Patients who have not received any periodontal therapies during past 6 months
Exclusion Criteria
Patients suffering from known systemic diseases like diabetes, cardiovascular, kidney disorders, Atherosclerosis.
Patients having alveolar destruction
Pregnant or lactating females
Immunocompromised patient, smokers, alcoholics
Patients who received any chemotherapeutic medicines during past 6 months
Patients who are contraindicated for virechana and gandoosha
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate the combined effect of virechana, pratisarana, gandusha in improving the symptoms, gingival bleeding index and plaque index in periodontitis. <br/ ><br> <br/ ><br>Restoration of normal microbial profile of saliva in periodontitis <br/ ><br>Timepoint: Subjective parameters, plaque and Gingival bleeding index score will be analysed at baseline visit, on 45th day (AT) and on each follow up visit (75th, 105th and 135th day). <br/ ><br> <br/ ><br> <br/ ><br>Saliva pH and microbial load will be assessed at time of baseline visit and on 45th day(AT). <br/ ><br>
- Secondary Outcome Measures
Name Time Method To understand the effectiveness of the treatment trial in preventing the recurrence of periodontitis.Timepoint: 75th, 105th and 135th day after completion of treatment trial.