Improving Symptoms of Dry Mouth in Sjogren's Syndrome Clinical Trial
Official title:
Rebamipide for the Treatment of Xerostomia in Sjögren Syndrome
Xerostomia is a major distressing symptom in Sjőgren's syndrome(SS). Preclinical and clinical studies have demonstrated an increase in saliva volume following rebamipide administration.We thus hypothesize that rebamipide may be efficacious in the treatment of dry mouth symptoms related to Sjőgren's syndrome.We will recruit SS patients in a randomized placebo-controlled trial for 12 weeks. The main outcome measure that will concern us is patient-assessed improvement of dry mouth symptoms and increase in salivary secretion Safety and efficacy was assessed at each visit.
Xerostomia is a major distressing symptom in Sjőgren's syndrome (SS). Persistent dryness of
the mouth causes oral pain, discomfort and significantly interferes with the quality of life.
Rebamipide, in addition to its gastro-protective effect has displayed various
anti-inflammatory actions including inhibition of neutrophilic leukocyte activation.
Preclinical and clinical studies have demonstrated an increase in saliva volume following
rebamipide administration.
The aim of the present study is to assess efficacy of rebamipide in the treatment of dry
mouth symptoms related to Sjőgren's syndrome.
Methods: Fifty-five patients with American European Consensus Criteria Group (AECG)-based
diagnosis of SS will participate in this randomized placebo-controlled trial. Inclusion
criteria will include SS patients with dry mouth symptoms. Patients with dry mouth due to
other conditions will be excluded. Patients will be randomized 1:1 to receive either 300mg/d
(100mg x3/day) of rebamipide or placebo for 12 weeks together with their usual therapy.
Outcome measures will include patient-assessed improvement of dry mouth symptoms and increase
in salivary secretion (evaluation of unstimulated saliva; questionnaires including the visual
analogue scale (VAS) for Sicca-syndrome VAS 0-100mm). Subjective and objective findings of
dry mouth will be recorded at baseline, two, four, six, eight, ten and twelve weeks. Safety
and efficacy will be assessed at each visit.
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