Trials / Completed
CompletedNCT02329600
Evaluation of Green Tea as Antioxidant Agent in Management of Oral Lichen Planus
Evaluation of Systemic Administration of Green Tea Polyphenols as a Supportive Antioxidant Agent in the Management of Oral Lichen Planus
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 40 (actual)
- Sponsor
- Cairo University · Academic / Other
- Sex
- All
- Age
- 30 Years – 68 Years
- Healthy volunteers
- Accepted
Summary
The study included forty individuals divided into 3 groups. 10 control subjects, 15 oral lichen planus (OLP) patients who were treated with topical corticosteroids and 15 oral lichen planus (OLP) patients who were treated with topical corticosteroids and green tea tablets.
Detailed description
This study included forty individuals divided into 3 groups. Group A; 10 systemically healthy control subjects not receiving medication. Group B; 15 Patients who were previously diagnosed with OLP presented in acute exacerbation were treated with topical corticosteroids; Triamcinolone acetonide (Kenalog in orabase: Bristol-Myers, Squibb, Spain) applied topically 4 times a day i.e. following each meal and at bed time for one month. Group C; 15 Patients who were previously diagnosed with OLP presented in acute exacerbation were treated with both topical corticosteroids; Triamcinolone acetonide (Kenalog in orabase: Bristol-Myers, Squibb, Spain) applied topically 4 times a day i.e. following each meal and at bed time for one month in addition to green tea tablets 200 mg (Green tea extract 5:1, El Obour For Modern Pharmaceutical Industries) as one tablet a day also for one month.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | green tea tablets (Green tea extract 5:1) 200 mg | Green tea is a product made from the Camellia sinensis plant. The fresh leaves are used to make medicine. the green tea extract is presented in a form of tablets 200 mg and is taken orally. |
| DRUG | Triamcinolone Acetonide | topical corticosteroids (Kenalog in orabase: Bristol-Myers, Squibb, Spain) applied topically 4 times a day i.e. following each meal and at bed time for one month |
Timeline
- Start date
- 2013-06-01
- Primary completion
- 2014-08-01
- Completion
- 2014-10-01
- First posted
- 2014-12-31
- Last updated
- 2016-11-15
- Results posted
- 2016-11-15
Source: ClinicalTrials.gov record NCT02329600. Inclusion in this directory is not an endorsement.