Minor Aphthous Ulcer.
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: The patient must be 20 to 40 years old Onset of the aphthous ulcers must not be more than one day No treatment must be applied for the aphthous lesions before visiting the school Patients must agree to participate and cooperate in this research Patients must not suffer from known systemic diseases associated with aphthous ulcers and they must not have suspected symptoms of systemic diseases associated with aphthous ulcers Lesions must be in the tonsils and 1.3 posterior of the mouth
Exclusion criteria
Exclusion criteria: Using another drug at the same time as the prescribed drug to treat the pest Not using the drug as recommended according to the patient's statements Not attending the School for re-examination Having symptoms of Behcet's disease (recurrent aphthous ulcers, recurrent genital lesions, skin and eye lesions)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The size of the lesion. Timepoint: Measurement of aphthous ulcer diameter at the beginning of the study and 3, 5 and 7 days after use of Teriadent and Ora-Aid Mucosal Adhesive. Method of measurement: The size of the lesion will be measured based on the maximum wound diameter using one-millimeter checkered paper. | — |
Secondary
| Measure | Time frame |
|---|---|
| Pain and irritation intensity. Timepoint: Measurement of pain and irritation intensity at the beginning of the study and 3, 5 and 7 days after use of Teriadent and Ora-Aid Mucosal Adhesive. Method of measurement: The patient's pain and irritation intensity will be measured according to the Visual Analogue Scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Yazd University of Medical Sciences