Recurrent Aphthous Stomatitis Clinical Trial
Official title:
Influence of Different Doses of the Vitamin B12 on Recurrent Aphthous Stomatitis
Background: The frequency of recurrent aphthous stomatitis (RAS), the most common oral
mucosa lesions seen in primary care, is up to 25% in the general population. Sublingual
vitamin B12 treatment, 1000 mcg per day for 6 months was found to be effective for patients
suffering from RAS, regardless of the serum vitamin B12 level. However, the optimal
therapeutic dose of vitamin B12 treatment remains unclear.
Working hypothesis and aims:
Aim-To assesses the influence of different vitamin B12 treatment doses on the frequency and
severity of RAS episodes.
Working hypothesis- The group receiving the higher dose of vitamin B12 treatment will have
the lower frequency and severity of RAS episodes; the reaction will be faster.
Methods: randomized, double blind, intervention study.
Study population: 75 patients in three groups (total of 225 patients):
Group I- will receive sublingual vitamin B12 treatment, 1000 mcg per day for 6 months Group
II- will receive sublingual vitamin B12 treatment, 100 mcg per day for 6 months Group I-
will receive sublingual vitamin B12 treatment, 2000 mcg per day for 6 months Study design:
Study participates will be followed through three study periods: The first period- three
months prior to receiving active treatment, the second period- six month of active treatment
(with randomization to study groups), and the third period- three month after finishing
active treatment. Frequency and severity of RAS episodes will be recorded by the patient
with "aphthous diary" that will be filled daily during all study period (12 months).
Expected results: This study will allow us to identify optimal dose of vitamin B12 treatment
that will achieve faster and longer remission of RAS episodes.
Importance: This is a very common problem in the population. Study results will help to
identify optimal doses of vitamin B12 needed to treat RAS.
Probable implications to Medicine: study results are supposed to give faster and better
treatment for RAS episodes
n/a
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver), Primary Purpose: Treatment
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