pimecrolimus versus placebo in minor, recurrent aphthous stomatitis: a randomized double-blind controlled trial
Authors
abstract
background: oral aphthous is one of the most common oral mucosal inflammatory disorders which are very painful. there is no definite medical strategy up to now for aphthous treatment. recently, some researchers have focused on immunomodulatory drugs such as tacrolimus and pimecrolimus in preventing aphthus recurrences. the aim of this study is to assess the effect of pimecrolimus cream against placebo in management of oral minor aphthous. methods: the study is a randomized clinical trial, was done in “shariati” hospital and isfahan skin research center. 62 patients with minor aphthuos were included and divided randomly to two groups (31 in each). in experimental group, pimecrolimus cream was applied for two weeks and cold cream for the same duration in control group. patients were followed for 3 and one week; results were assessed in recovery after drug administration. compared variables between two groups were including: the size of lesions, the time to recovery and pain intensity. results: results showed that mean size lesion in experimental and placebo group after complete recovery reduced (23.6 ±15.3 and 24.8 ±15 mm respectively) but it was not significant (p: 0.1). mean time for recovery in both groups was 8±2.2 and 9.5±2.5 respectively which was significant in pimecrolimus treated patients (p: 0.014). also mean degree for pain intensity measured by pain scale method was reduced significantly in test group (6 ± 1.2 before treatment and 5.3 ± 1.1 after treatment, p<0.001). conclusion: this study stated that pimecrolimus cream has an appropriate effect in reduction of recovery time and pain in minor aphthous compared to placebo but more clinical studies are needed to better conclusion.
similar resources
A randomized, double-blind, placebo-controlled trial of pentoxifylline for the treatment of recurrent aphthous stomatitis.
OBJECTIVE To evaluate pentoxifylline for the treatment of recurrent aphthous stomatitis. DESIGN A 60-day, randomized, double-blind, placebo-controlled trial with a 60-day no treatment follow-up. SETTING An oral medicine specialist referral center in Manchester. PARTICIPANTS Forty-nine volunteers who passed the initial assessment for recurrent aphthous stomatitis entered a pretrial phase i...
full textComparison of colchicine versus prednisolone in recurrent aphthous stomatitis: A double-blind randomized clinical trial.
PURPOSE Recurrent aphthous stomatitis (RAS) is one of the most common ulcers of the oral cavity with a reported prevalence of 5- 50%. There is still no definitive treatment for RAS; however, immunosuppressive and immunomodulant agents have been proposed. In this study, we compared the therapeutic effects of 5 mg/d prednisolone with 0.5 mg/d colchicine in the treatment of RAS. METHODS In a dou...
full textRe: Effectiveness of vitamin B(12) in treating recurrent aphthous stomatitis: a randomized, double-blind, placebo-controlled trial.
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. However, there has been no optimal therapeutic approach. Our objective was to confirm our previous clinical observation of the beneficial treatment of RAS with vitamin B(12). METHODS A randomized, double-blind, placebo-controlled tr...
full textCurcumin Gel in the Treatment of Minor Aphthous Ulcer: a Randomized, Placebo- Controlled Trial
Background: It has been reported that curcumin has anti inflammatory, antibacterial, anti tumor and analgesic properties. Objective: The purpose of this study was to investigate the efficacy of curcumin in the treatment of minor aphthous stomatitis. Methods: The study was a two week, randomized, double blind, placebo controlled of patients with minor aphthous. Patients between 18 and 65 years...
full textA Randomized, Double-Blind, Placebo-Controlled Trial
Results: The cumulative number of gadoliniumenhancing MRI lesions during the first 6 months were similar in the -3 fatty acids and placebo groups (median difference, 1; 95% CI, 0 to 3; P=.09). No difference in relapse rate was detected after 6 (median difference, 0; 95% CI, 0 to 0; P=.54) or 24 (median difference, 0; 95% CI, 0 to 0; P=.72) months. The proportion of patients without disability p...
full textA Randomized, Placebo-Controlled Double-Blind Trial
The efficacy and safety of pentoxifylline were assessed in 297 adult patients with ischemic stroke in a molticenter, doable-blind, randomized and placebo-controlled trial. Treatment was started within 12 hoars after the stroke onset Study medication was administered intravenously continuously (16 mg/kg/day, maximum 1,200 mg/day) for 3 days and per os (400 mg ti.d.) for the remainder of 28 days....
full textMy Resources
Save resource for easier access later
Journal title:
journal of pharmaceutical careجلد ۲، شماره ۱، صفحات ۱۰-۱۴
Hosted on Doprax cloud platform doprax.com
copyright © 2015-2023