Stomatitis. Stomatitis and related lesions
Conditions
Interventions
Intervention 1: Case 1: a experimental group solution containing extract yarrow-routine solution (2 dexamethasone 8 mg, 5 tablets sucralfate 500 mg, 1 syrup diphenhydramine 12.5 mg, 1 injection of lid
Treatment - Drugs
Case 1: a experimental group solution containing extract yarrow-routine solution (2 dexamethasone 8 mg, 5 tablets sucralfate 500 mg, 1 syrup diphenhydramine 12.5 mg, 1 injection of lidocaine 2%) (glas
Case 2: a control group routine solution containing (2 dexamethasone 8 mg, 5 tablets sucralfate 500 mg, 1 syrup diphenhydramine 12.5 mg, 1 injection of lidocaine 2%) (glass 2) is given will. Patients
Sponsors
Vice chancellor for research, Kashan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
1 Years to 149 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: informed consent for participation in the study, aged 20 years and older, no underlying disease (allergy, allergic rhinitis, asthma ), not receive radiation therapy after diagnosis, having consciousness, not use another mouthwash solution during the study, and not receiving systemic antibiotics and antifungals. Exclusion criteria: receiving radiotherapy during treatment, fever, use from another solution mouthwash during the study, the decision to withdraw from the study, irregular use of mouthwash solution (frequency, amount), solution containing extract yarrow odor intolerance by patients and received systemic antibiotics and antifungals at the beginning or during the study.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Stomatitis. Timepoint: Before and seventh and fourteenth days after the intervention. Method of measurement: Standardized checklist stomatitis WHO. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactLeyla Soleymanpoor
Kashan University of Medical Sciences
Outcome results
None listed