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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03475394
Other study ID # KLEU/Ethic/14-15/D-79
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 2015
Est. completion date November 2015

Study information

Verified date October 2022
Source KLE VK Institute of Dental Sciences
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Description:

Morus alba is invaluable member of the plant kingdom belonging to the family Moraceae and the genus Morus. It is extensively cultivated for leaf yield in sericulture. Morus alba have long been used in traditional medicine to improve eyesight, lower blood pressure, prevent diabetes, protect the liver, strengthen joints and treat fever. In particular, few studies on mulberry fruits have reported its biological activities such as antioxidative and anti-inflammatory activities. Even the root bark of has been traditionally used in Asian countries for medicinal purposes due to its anti-inflammatory, hypoglycemic, antibacterial activities. LD50 of extracts of Morus Alba leaves was found to be above 2000 mg/kg which is safe to be used in human beings. Therefore, in the present study the Morus alba leaves has been used in the gel preparation and its effectiveness is assessed against periodontal microorganisms.


Recruitment information / eligibility

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

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Chlorhexidine gel
0.1 ml of Chlorhexidine gel was administered into the periodontal pocket
Morus alba gel
0.1 ml of Morus alba gel was administered into the periodontal pocket
Placebo
0.1 ml of Placebo gel was administered into the periodontal pocket

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
KLE VK Institute of Dental Sciences

Outcome

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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