recurrent aphthous stomatitis. Recurrent oral aphthae
Conditions
Interventions
Intervention 1: Intervention group:20 patients with oral aphthous receive a solution of ANCIL at a dose of 0.5 twice a day. Intervention 2: Intervention group: 20 patients with oral aphthous receive a
Sponsors
Tabriz University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 40 Years
Inclusion criteria
Inclusion criteria: Minor and solitary aphthous ulcers in the lip mucosa or cheek Age range 18 to 40 years
Exclusion criteria
Exclusion criteria: Pregnant Breastfeeding Patients with systemic disease Patients with herpetiform ulcers and multiple major or minor aphthous ulcers for more than 4 days Patients who refuse to participate in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Comparison of different doses of ANCIL and placebo solution on the recovery time of recurrent oral aphthous. Timepoint: 80 patients will be divided into 4 groups of 20 and 3 groups of patients will receive doses of 0.5, 1, and 2 ANCIL solution. The fourth group will receive the basic formulation of the solution without active components. The duration of use of the solutions will be a maximum of 7 days. Then the duration of complete recovery of the oral aphthous in the groups will be compared. Method of measurement: Different doses are compared based on the patient's clinical symptoms and observing the speed of oral aphthous recovery.;Pain intensity in patients with recurrent oral aphthous. Timepoint: On days 0, 5 and 7. Method of measurement: VAS questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAli Yousefipour
Tabriz University of Medical Sciences
Outcome results
None listed