Evaluation the effect of a synthetic mouthwash on the oral ulcers pain and size
Phase 2
Recruiting
- Conditions
- oral ulcer.K12.39Other oral mucositis (ulcerative)
- Registration Number
- IRCT20120101008585N5
- Lead Sponsor
- Shiraz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
The patient who has painful new oral lesion without receiving any treatment
The patients who are not pregnant
The patients who are not diabetic
The patients with no other inflammatory diseases
The patients who sign the written consent form
Exclusion Criteria
The patients who have used any analgesic agents (systemic or local) since 2 days ago
The patients who have used any anti-inflammatory medication such as corticosteroid since 2 weeks ago
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method evel of pain. Timepoint: after gargling these analgesics agent for 5 minute, VAS of patients will be measured in 5, 15, 30 and 1 hour intervals. Their VAS will be measured after each gargling also in day 1,2,3. Method of measurement: visual analogue scale.;The size of oral ulcer. Timepoint: The size of oral lesions will be measured after gargling in day 1,2,3 in intervention and control groups. Method of measurement: scaled tongue blade.
- Secondary Outcome Measures
Name Time Method The side effects of using mouth washes. Timepoint: day 1,2,3 and a week after using mouth wash. Method of measurement: asking the patient.