Periodontal Diseases Clinical Trial
Official title:
Evaluation of Anti-plaque Effect of a Mouthwash Composed of Salvadora Persica L. and Green Tea: a 4days Randomized Controlled Crossover Clinical Trial
Verified date | May 2019 |
Source | University of Baghdad |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Periodontal diseases and caries are essentially initiated and progressed by accumulation of dental plaque. Thus, daily effective plaque control is valuable as a preventive measure and maintaining oral health. Mechanical plaque control is important but has limitations; therefore, an adjunctive chemical plaque control such as mouthwash is helpful. Various medicinal plant-derived galenicals might be used as safe and stable alternatives to synthetic mouthwashes. For example, a combination of Salvadora persica L. (Sp) root sticks and green tea (Gt) aqueous extract has been found to reduce plaque accumulation over 24 hours. Moreover, these extracts were reported to have anti-microbial activity against many oral bacteria. The objective of this study was to investigate the efficacy of the combination of Gt aqueous extract and Sp aqueous extract in reducing plaque buildup for 4 days duration.
Status | Completed |
Enrollment | 15 |
Est. completion date | April 9, 2019 |
Est. primary completion date | March 31, 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 20 Years to 23 Years |
Eligibility |
Inclusion Criteria: - Participants should be medically healthy. - Participants should have more than 20 teeth. Exclusion Criteria: - Participants who have active cavity caries and/or periodontal disease. - Participants who have ongoing orthodontic treatment. - Participants who have been on antibiotics within the past 4 months. - Participants who require prophylactic antibiotic coverage. - Participants who have been on systemic or topical non-steroidal anti-inflammatory drugs for the past 4 months. - Participants who are pregnant or intended to and lactating mother. - Participants who have heart valve replacement and have known intolerance or allergy to mouth rinses. - Participants who have any systemic disease. |
Country | Name | City | State |
---|---|---|---|
Iraq | Hayder R Abdulbaqi | Baghdad |
Lead Sponsor | Collaborator |
---|---|
University of Baghdad |
Iraq,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Mean amount plaque between different comparators | Mean amount plaque between different comparators as anti-plaque agent following 24 hrs plaque regrowth clinical trial by means of modified quigely hein plaque index [Turesky, 1970] and digital plaque image analysis. | Time Frame: 24 hours | |
Primary | Mean amount plaque between different comparators | Mean amount plaque between different comparators as anti-plaque agent following 4 days plaque regrowth clinical trial by means of modified quigely hein plaque index [Turesky, 1970] and digital plaque image analysis. | Time Frame: 4 days | |
Secondary | Mean bacterial load in saliva | Mean bacterial load in saliva at 2 hours after rinsing with different comparators using quantitative polymerase chain reaction (qPCR). | 2 hours | |
Secondary | Mean relative changes in gingival crevicular fluid flow rate | Mean relative changes in gingival crevicular fluid flow rate after rinsing with different comparators from baseline at 4 days. | 4 days | |
Secondary | Mean relative changes in Interleukin1 beta levels in gingival crevicular fluid | Mean relative changes in Interleukin1 beta levels in gingival crevicular fluid after rinsing with different comparators from baseline at 4 days. | 4 days |
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