Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ENROLLING_BY_INVITATION
PHASE1/PHASE2
30 participants
INTERVENTIONAL
2024-10-12
2025-03-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Thyme Honey group
Topical application of Thyme Honey
thyme honey
Topical application on the oral mucosa
Control group
Topical application of Triamcinolone acetonide
Triamcinolone Acetonide
Topical application on the oral mucosa
Interventions
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thyme honey
Topical application on the oral mucosa
Triamcinolone Acetonide
Topical application on the oral mucosa
Eligibility Criteria
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Inclusion Criteria
* Patients who agreed to take supplied medications.
* Patients who agreed for the biopsy (when required).
Exclusion Criteria
* Treatment with any oral topical medications for at least four weeks prior to the study.
* Pregnant and lactating women.
* In addition, no consideration was given to patients with a history of hypersensitivity to honey.
ALL
No
Sponsors
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British University In Egypt
OTHER
Responsible Party
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Locations
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The British university in Egypt
Cairo, , Egypt
Countries
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Other Identifiers
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24-092
Identifier Type: -
Identifier Source: org_study_id
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