Chronic Periodontitis Clinical Trial
Official title:
Comparison of Effectiveness of Morus Alba and Chlorhexidine Gels on Moderate Periodontitis Among 35 to 55 Year Old Subjects: A Hospital Based Randomized Controlled Trial
Verified date | October 2022 |
Source | KLE VK Institute of Dental Sciences |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Background: Periodontitis is a chronic inflammatory disease of tooth and supporting tissues with clinical signs of bone and connective tissue loss and is mediated by a combination of periodontal pathogens and host defense systems. Currently the use of herbal products in dentistry is increasing due to their easy availability, low cost and lesser side effects. One such herbal plant is Morus alba which is known to possess medicinal properties. Therefore the present study was conducted to determine the clinical effectiveness of subgingivally delivered Morus alba gel incorporated into polaxamers vehicle for its controlled release on periodontal pocket in adjunct to scaling and root planing for treatment of moderate periodontitis patients. Methods: one hundred eighty patients with chronic periodontitis having pocket depth of ≥5 mm in atleast two different teeth were treated by full-mouth scaling and root planning (SRP) and curettage. They were randomly assigned into one of the three groups with 60 in each group: Group 1: Chlorhexidine Sol-gel was applied at baseline, 15 and 30 days. Group 2: Morus alba Sol-gel was applied at baseline, 15 and 30 days. Grpup 3: Placebo gel was applied at baseline, 15 and 30 days. Plaque index (PI) (Silness and Loe), Gingival index (GI) (Loe and Silness), Community Periodontal index, Periodontal pocket depth and quantitative analysis (anaerobic culture) of Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis and Tannerella forsythia were assessed at baseline and after 45 days.
Status | Completed |
Enrollment | 180 |
Est. completion date | November 2015 |
Est. primary completion date | September 2015 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 35 Years to 55 Years |
Eligibility | Inclusion Criteria: 1. 35 to 55 years old 2. untreated moderate chronic periodontitis having probing pocket depth of =5 mm in atleast two different teeth Exclusion Criteria: 1. use of antibiotics or anti-inflammatory drugs during the last 6 months before baseline examination 2. Received periodontal treatment in the last 6 months 3. pregnant or lactating 4. allergy to chlorhexidine or any of the components in the tested products 5. using tobacco products in any form 6. systemic diseases (e.g., diabetes mellitus, hypertension and immunological disorders) 7. ) orthodontic treatment 8. alcoholics 9. removable prostheses 10. Healthy with a normal BMI |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
KLE VK Institute of Dental Sciences |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Reduction in the periodontal pocket depth | Measured by Probing pocket depth | 45 days | |
Secondary | Reduction in the Microbial count of periodontal pathogens | Reduction in Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis and Tannerella forsythia | 45 days | |
Secondary | Reduction in Plaque deposition | Measured by Plquel index (Silness and Loe) | 45 days | |
Secondary | Reduction in gingival inflammation | Measured by Gingival index (Loe and Silness) | 45 days |
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