Aphthous Stomatitis. Aphthous stomatitis
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: No more than 2 days have passed since the onset of aphthous ulcers. Have not used any other treatment for their wounds before going to the clinic. Patients have completed the consent to participate in the trial. Be in the age group over 18 years. People with a clear history of plague should be reported at least twice a year.
Exclusion criteria
Exclusion criteria: People are allergic to the compounds and drugs used in the trial. Failure to follow the recommended instructions during the study Patients with systemic diseases such as diabetes, asthma, renal and hepatic insufficiency, epilepsy, blood and glandular disorders as well as pregnant women Patients taking antibiotics or anti-inflammatory drugs for other reasons.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Follow-up time to observe changes and improvement in aphthous lesions will be on days zero (during the first visit to the doctor), 1 (first examination) on days 7 and 10 (follow-up) after starting treatment, which will be done by referring patients to the clinic. The studied variables include the number of wounds, the size of the wounds, the amount of pain and burning, and the amount of erythema and exudate. This information will be recorded each time the patient is examined in a special form along with the patient's demographic information. Timepoint: Follow-up time to observe changes and improvement in aphthous lesions will be on days zero (during the first visit to the doctor), 1 (first examination) on days 7 and 10 (follow-up) after starting treatment, which will be done by referring patients to the clinic. Method of measurement: Wound size will be measured by a special Williams dental probe. Also, the number of mouth ulcers will be counted at the beginning of the day and during the study period. The scale of burning and pain consists of a line of 10 cm, which means zero, no pain and 10 maximum pain. The patient determines the points that indicate pain, then from zero to that point will be measured and a numerical scale from one to 100 mm will be recorded.Pain intensity in patients will be measured based on the Visual Analog Scale (VAS). This pain scale represents a 10 cm line printed with markers at each end on a piece of paper. It is "painless" at one end and "worst pain" or "indescribable pain" at the other. The person places a cross × on the line to indicate the severity of their pain. A doctor then measures the line with a ruler to get a pain score.For children, pain scales using face images are commonly used. A child may express pain with pictures of eight different faces with different expressions. The child chooses a face that feels more in tune with their current level of pain. | — |
Countries
Iran (Islamic Republic of)
Contacts
Sanandaj University of Medical Sciences