Comparative Evaluation of Antiplaque and Antigingivitis Efficacy of Ocimum Sanctum (Tulsi) Extract
Primary Purpose
Periodontal Diseases, Gingivitis, Periodontitis
Status
Completed
Phase
Not Applicable
Locations
India
Study Type
Interventional
Intervention
Ocimum sanctum
Chlorhexidine Gluconate
Propylene Glycol
Sponsored by
About this trial
This is an interventional prevention trial for Periodontal Diseases focused on measuring Mouthrinse, Ocimum sanctum, Periodontal Diseases, Tulsi
Eligibility Criteria
Inclusion criteria
- Cases with generalized chronic gingivitis or cases with mild generalized chronic periodontitis patients of any sex.
- Systemically healthy individuals.
- Participants having >20 teeth.
- Participants in the age group of 18-40 years, who abide by approved protocol guidelines, and are ready to give written informed consent.
Exclusion criteria
- Any known systemic disease which has effects on periodontium such as diabetes, cardiovascular, cancer etc.
- Participants on anti-inflammatory, perioceutics, antibiotics, steroids, cytotoxic and drugs since 03 months.
- Participants who have known allergy to material used for the study.
- Pregnant and lactating mothers.
- Participants had undergone any kind of nonsurgical and/or surgical periodontal therapy earlier, in past 6 months.
- Tobacco users (smoke and smokeless) and alcoholics.
- Participants wearing any form of intraoral prosthesis or appliance.
Sites / Locations
- GCD Indore
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Active Comparator
Placebo Comparator
Arm Label
Ocimum sanctum extract as mouthrinse
Chlorhexidine Gluconate as mouthrinse
Propylene Glycol as mouthrinse
Arm Description
10ml mouthrinse was rinsed for 60sec twice a daily for 03 weeks.
10ml mouthrinse was rinsed for 60sec twice a daily for 03 weeks.
10ml mouthrinse was rinsed for 60sec twice a daily for 03 weeks.
Outcomes
Primary Outcome Measures
Modified Gingival Index
The Modified Gingival Index (Lobene, Weatherford, Ross, Lamm, 1986) was recorded based on following criteria: 0 - Absence of inflammation. 1 - Mild inflammation or with slight changes in color and texture but, not in all portions of marginal or papillary gingiva. 2 - Mild inflammation, such as the preceding criteria, in all portions of marginal or papillary gingiva. 3 - Moderate, bright surface inflammation, erythema, edema, and/or hypertrophy of marginal or papillary gingiva. 4 - Severe inflammation: erythema, edema and/or marginal gingival hypertrophy of the unit or spontaneous bleeding, papillary, congestion or ulceration. Modified Gingival Index = Total score of all teeth / no. of sites
Secondary Outcome Measures
Modified Plaque Index
Plaque Index (Turesky, Gilmore, Glickman modification of Quigely Hein Index, 1970) Scoring was as follows: 0 - No plaque/debris. 1 - Separate flecks of plaque at the cervical margin of the tooth. 2 - A thin continuous band of plaque (up to 1mm) at the cervical margin of the tooth. 3 - A band of plaque wider than 1 mm but covering less than one third of the crown of the tooth. 4 - plaque covering at least one third but less than two thirds of the crown of the tooth. 5 - Plaque covering two third or more of the crown of the tooth. Plaque Index = Total score / no. of surfaces examined
Full Information
NCT ID
NCT03474146
First Posted
March 8, 2018
Last Updated
April 16, 2018
Sponsor
Government College of Dentistry, Indore
1. Study Identification
Unique Protocol Identification Number
NCT03474146
Brief Title
Comparative Evaluation of Antiplaque and Antigingivitis Efficacy of Ocimum Sanctum (Tulsi) Extract
Official Title
"Comparative Evaluation of Antiplaque and Antigingivitis Efficacy of Ocimum Sanctum (Tulsi) Extract Mouthrinse With 0.12% Chlorhexidine Mouthrinse - an in Vitro and in Vivo Study."
Study Type
Interventional
2. Study Status
Record Verification Date
April 2018
Overall Recruitment Status
Completed
Study Start Date
April 12, 2017 (Actual)
Primary Completion Date
July 22, 2017 (Actual)
Study Completion Date
July 31, 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Government College of Dentistry, Indore
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Chlorhexidine is considered as gold standard for its antiplaque and antigingivitis efficacy till date but it has got many side effects. So it is need of the hour that investigators will find some substitute having similar antiplque and antigingivitis efficay but have less or no adverse effects. so in this study investigators planned to do "Comparative evaluation of antiplaque and antigingivitis efficacy of ocimum sanctum (tulsi) extract mouthrinse with 0.12% chlorhexidine mouthrinse.
Detailed Description
Title:
"Comparative evaluation of antiplaque and antigingivitis efficacy of ocimum sanctum (tulsi) extract mouthrinse with 0.12% chlorhexidine mouthrinse - an in vitro and in vivo study."
Aims And Objectives:
To evaluate the antimicrobial activity of Ocimum sanctum (Tulsi) extract by Sensitivity testing, Minimum Inhibitory Concentration, Minimum Bactericidal Concentration, and Time kill curve -In Vitro study.
To evaluate the Antiplaque and Antigingivitis effect of the Ocimum sanctum (Tulsi) by recording Modified Gingival Index and Modified Plaque Index in patients with Chronic Generalized Gingivitis and Mild Chronic Generalized Periodontitis -In Vivo study.
Clinical evaluation and comparison of the Antiplaque and Antigingivitis effect of the Ocimum sanctum (Tulsi) with 0.12% Chlorhexidine and vehicle.
To see the topical beneficial and/or harmful side effects of Ocimum sanctum extract, if any.
Study Design:
Prospective randomized controlled Trial- Randomized Comparative Study
Methodology (Material & Methods):
The present study will have following parts:
Procurement of extract and formulation of mouthrinse: Ocimum sanctum (Tulsi) extract has been purchased from the ISO (International Organization for Standardization) Certified shop. The desired mouthrinse will be formulated under the guidance of Department of Pharmacology, Mahatma Gandhi Memorial Medical College, Indore (M.P.)
In vitro study: Sensitivity testing, Minimum Inhibitory Concentration (MIC) and Minimum Bactericidal Concentration (MBC), of Ocimum sanctum will be determined against following microorganisms: Porphyromonas gingivalis, Prevotella intermedia, Fusobacterium nucleatum, Aggregatibacter actinomycetemcomitans, Capnocytophaga, Tannerella forsythia, Pseudomonas aeruginosa, and other microorganisms.
In vivo study: This study has been planned and would be conducted in the Department of Periodontology, Govt. College of Dentistry, Indore, Madhya pradesh, India. In this study, participants with Chronic Generalized Gingivitis and Mild Chronic Generalized Periodontitis would be randomly selected from outdoor patients. A minimum 90 Recruited participants will be divided into three equal groups randomly. (Parallel design, case control, Randomized Comparative Study).
Group A: (Test group) (n=30) Ocimum sanctum extract as mouthrinse. Group B: (Positive control group) (n=30) 0.12% Chlorhexidine as mouthrinse. Group C: (control group) (n=30) Vehicle as the mouthrinse. All the three solutions would be prepared under the valuable guidance of Department of Pharmacology, Mahatma Gandhi Memorial Medical College, Indore (M.P.) and will be kept in coded containers. All the participants in each group would be advised to use their respective mouth rinses twice daily with proper swishing action for a minute, after brushing their teeth (in the morning and before going to bed). To maintain standardization, similar toothbrushes and dentifrices will be provided to all the participants (free of cost) and standard tooth brushing techniques will be demonstrated.
Written consent will be obtained from each participants, and then followed by case history taking along with clinical examination by recording various periodontal parameters taken in the study.
Following clinical periodontal parameters are to be recorded at baseline, at 1 week, at 2 weeks, and at 3 weeks:
Modified Gingival Index
Modified Plaque Index
Sample Size:
Minimum 90 patients with Generalized Chronic Gingivitis or Mild Generalized Chronic Periodontitis will be selected. Participants will be divided into 03 different groups, n=30 participants in each group by computer generated table of random numbers.
Data Collection And Methods:
Cases with Generalized Chronic Gingivitis or Mild Generalized Chronic Periodontitis of either sex and the age group 18-40 years who abide by approved protocol guidelines and are ready to give written informed consent will be selected randomly from OPD (outpatient department) of The Department of Periodontology, Govt. College of Dentistry, Indore (M.P.). The selected participants will be equally divided into three groups, by computer generated random number table.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Periodontal Diseases, Gingivitis, Periodontitis
Keywords
Mouthrinse, Ocimum sanctum, Periodontal Diseases, Tulsi
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
90 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Ocimum sanctum extract as mouthrinse
Arm Type
Experimental
Arm Description
10ml mouthrinse was rinsed for 60sec twice a daily for 03 weeks.
Arm Title
Chlorhexidine Gluconate as mouthrinse
Arm Type
Active Comparator
Arm Description
10ml mouthrinse was rinsed for 60sec twice a daily for 03 weeks.
Arm Title
Propylene Glycol as mouthrinse
Arm Type
Placebo Comparator
Arm Description
10ml mouthrinse was rinsed for 60sec twice a daily for 03 weeks.
Intervention Type
Other
Intervention Name(s)
Ocimum sanctum
Other Intervention Name(s)
Tulsi, Holy Basil
Intervention Description
Ocimum sanctum (known as Tulsi, Holy basil) is natural herb which is known for its broad spectrum medicinal properties. Ocimum sanctum is one of the best examples of Ayurveda's holistic lifestyle approach to health. It is also been well practiced in traditional medicine in India and south Asian region. Literature showed that Ocimum sanctum extract have significant anti-gingivitis and anti-inflammatory effect as mouthrinse.
Intervention Type
Other
Intervention Name(s)
Chlorhexidine Gluconate
Other Intervention Name(s)
Chlorhexidine
Intervention Description
Chlorhexidine Gluconate (C34H54Cl2N10O14) is a bisbiguanide formulation with cationic properties. Chlorhexidine over a period of over 40 years has been thoroughly investigated and successfully used as plaque control agent in dental practice. A literature review, highlighting chlorhexidine as not only a plaque control agent but also as an effective antimicrobial agent and its wider application in variety of oral disorders in various formulations.
Intervention Type
Other
Intervention Name(s)
Propylene Glycol
Intervention Description
Propylene glycol or 1,2-dihydroxypropane or 1,2-propanediol, is a clear, colourless, viscous, practically odourless liquid with a density of 1.038 g/cm³ at 20 °C and a molecular weight of 76.095. It is miscible with water, acetone and chloroform. It is miscible in water. Propylene glycol is commonly used as an excipient in a variety of drugs and it is also authorised in food products and cosmetics.
Primary Outcome Measure Information:
Title
Modified Gingival Index
Description
The Modified Gingival Index (Lobene, Weatherford, Ross, Lamm, 1986) was recorded based on following criteria: 0 - Absence of inflammation. 1 - Mild inflammation or with slight changes in color and texture but, not in all portions of marginal or papillary gingiva. 2 - Mild inflammation, such as the preceding criteria, in all portions of marginal or papillary gingiva. 3 - Moderate, bright surface inflammation, erythema, edema, and/or hypertrophy of marginal or papillary gingiva. 4 - Severe inflammation: erythema, edema and/or marginal gingival hypertrophy of the unit or spontaneous bleeding, papillary, congestion or ulceration. Modified Gingival Index = Total score of all teeth / no. of sites
Time Frame
Change from baseline Gingival index at 03 weeks
Secondary Outcome Measure Information:
Title
Modified Plaque Index
Description
Plaque Index (Turesky, Gilmore, Glickman modification of Quigely Hein Index, 1970) Scoring was as follows: 0 - No plaque/debris. 1 - Separate flecks of plaque at the cervical margin of the tooth. 2 - A thin continuous band of plaque (up to 1mm) at the cervical margin of the tooth. 3 - A band of plaque wider than 1 mm but covering less than one third of the crown of the tooth. 4 - plaque covering at least one third but less than two thirds of the crown of the tooth. 5 - Plaque covering two third or more of the crown of the tooth. Plaque Index = Total score / no. of surfaces examined
Time Frame
Change from baseline Plaque index at 03 weeks
Other Pre-specified Outcome Measures:
Title
Minimum Inhibitory Concentration (MIC)
Description
Minimum inhibitory concentration (MIC) is the lowest concentration of a chemical which prevents visible growth of a bacterium. Tested against following periopathogens: Porphyromona sgingivalis, Prevotella intermedia, fusobacteriumnucleatum, Aggregatibacter actinomycetemcomitans, Capnocytophaga, Tanerella forsythia, Pseudomonas aeruginosa, Streptococcus mutans, E. fecalis, and Candida.
Time Frame
Up to 24 hours
Title
Minimum bactericidal concentration (MBC)
Description
Minimum bactericidal concentration (MBC) is the concentration resulting in microbial death as defined by the inability to re-culture bacteria. Tested against following periopathogens: Porphyromona sgingivalis, Prevotella intermedia, fusobacteriumnucleatum, Aggregatibacter actinomycetemcomitans, Capnocytophaga, Tanerella forsythia, Pseudomonas aeruginosa, Streptococcus mutans, E. fecalis, and Candida.
Time Frame
Up to 24 hours
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion criteria
Cases with generalized chronic gingivitis or cases with mild generalized chronic periodontitis patients of any sex.
Systemically healthy individuals.
Participants having >20 teeth.
Participants in the age group of 18-40 years, who abide by approved protocol guidelines, and are ready to give written informed consent.
Exclusion criteria
Any known systemic disease which has effects on periodontium such as diabetes, cardiovascular, cancer etc.
Participants on anti-inflammatory, perioceutics, antibiotics, steroids, cytotoxic and drugs since 03 months.
Participants who have known allergy to material used for the study.
Pregnant and lactating mothers.
Participants had undergone any kind of nonsurgical and/or surgical periodontal therapy earlier, in past 6 months.
Tobacco users (smoke and smokeless) and alcoholics.
Participants wearing any form of intraoral prosthesis or appliance.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dr. Subhash Garg, M.D.S.
Organizational Affiliation
Govt. College of Dentistry, Indore, Madhya pradesh, India
Official's Role
Study Director
Facility Information:
Facility Name
GCD Indore
City
Indore
State/Province
Madhya Pradesh
ZIP/Postal Code
452001
Country
India
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
24948862
Citation
Gupta D, Bhaskar DJ, Gupta RK, Karim B, Jain A, Singh R, Karim W. A randomized controlled clinical trial of Ocimum sanctum and chlorhexidine mouthwash on dental plaque and gingival inflammation. J Ayurveda Integr Med. 2014 Apr;5(2):109-16. doi: 10.4103/0975-9476.131727.
Results Reference
background
PubMed Identifier
3485495
Citation
Lobene RR, Weatherford T, Ross NM, Lamm RA, Menaker L. A modified gingival index for use in clinical trials. Clin Prev Dent. 1986 Jan-Feb;8(1):3-6. No abstract available.
Results Reference
background
PubMed Identifier
5264376
Citation
Turesky S, Gilmore ND, Glickman I. Reduced plaque formation by the chloromethyl analogue of victamine C. J Periodontol. 1970 Jan;41(1):41-3. doi: 10.1902/jop.1970.41.41.41. No abstract available.
Results Reference
background
Learn more about this trial
Comparative Evaluation of Antiplaque and Antigingivitis Efficacy of Ocimum Sanctum (Tulsi) Extract
We'll reach out to this number within 24 hrs