Aphthous stomatitis. Recurrent oral aphthae
Conditions
Interventions
Intervention 1: Control group: Triadent 0.1%, one centimeter of gel three times a day, until complete healing of wounds and pain on days 0, 1, 3 and 5 marked in the VAS (Visual Analogue Scale) questio
Sponsors
Esfahan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 50 Years
Inclusion criteria
Inclusion criteria: Minimum age 18 years Non-pregnant and non-breastfeeding women The patient's ability to stay on during the study period.
Exclusion criteria
Exclusion criteria: Pregnancy Breastfeeding women People who are sensitive to herbal products Systemic patients such as:, patients with primary or acquired immunodeficiency Patients with a history of taking anti-inflammatory drugs and corticosteroids Major aphthous ulcers and Herpetiform Wounds with durability longer than 48 hours
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Size of wound. Timepoint: The first, third and fifth days after the intervention. Method of measurement: Ruler.;Pain. Timepoint: Before the study, the first, third and fifth days after the start of the study. Method of measurement: Visual Analogue Scale.;Healing ulcer. Timepoint: Before start and after end of the study. Method of measurement: Examination. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAtefeh Tavangar
Esfahan University of Medical Sciences
Outcome results
None listed