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Clinical Trial Summary

use seseme oil and corticosteroid topically for two groups


Clinical Trial Description

- The enrolled patients will be divided randomly into two groups.

- Test group will receive topical sesame oil (3 times /day after eating) for a month.

- Control group will receive topical corticosteroid (3 times /day after eating) for a month.

- Assessment of the appearance score and severity of pain as well as the clinical parameter outcome will be done at baseline and at the end of two and four weeks and will be recorded in the patients' questionnaires & by clinical sign score . MDA will be measured at the baseline & at the end of four weeks after treatment. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03738176
Study type Interventional
Source Cairo University
Contact Mona Taha Mohammed Ahamed, Master
Phone 01123294474
Email mona.taha@dentistry.cu.edu.eg
Status Not yet recruiting
Phase Early Phase 1
Start date December 16, 2019
Completion date December 30, 2020

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