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Stomatitis, Aphthous clinical trials

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NCT ID: NCT02142543 Completed - Clinical trials for Minor Recurrent Aphthous Stomatitis Lesions

The Effect of 2-DeNT Oral Topical Powder on Minor Recurrent Aphthous Ulcer

Start date: March 2012
Phase: Phase 0
Study type: Interventional

This is a prospective, randomized, blinded, placebo-controlled, crossover clinical trial to evaluate the efficacy of 2-DeNT oral topical powder in the treatment of recurrent aphthous stomatitis (RAS). To be included in the study, subjects must have had minor RAS ulcers of less than 48 hours duration. It was randomly determined which powder was used first; all subjects used both the 2-DeNT powder and the placebo powder. Subjects applied the powder twice daily and maintained a daily log recording the size of the ulcer, its erythema score, and their level of pain. The subjects continued applying the 2-DeNT powder until the ulcer was resolved.

NCT ID: NCT01831453 Active, not recruiting - Clinical trials for Recurrent Mouth Ulcers

Omega-3 and Quality of Life in Recurrent Aphthous Stomatitis Patients

Start date: April 2012
Phase: Phase 2
Study type: Interventional

The study aims at evaluating the effect of omega-3 on patients suffering recurrent oral aphthous ulcers

NCT ID: NCT01652625 Completed - Clinical trials for Recurrent Aphthous Stomatitis

Efficacy and Safety Study of Yunnan Baiyao on Minor Recurrent Aphthous Stomatitis

Start date: March 2010
Phase: Phase 2
Study type: Interventional

Recurrent aphthous stomatitis (RAS) is a common recurrent oral disorder with no curative treatment available to date. The challenge remains in patients that do develop drug resistance and/or secondary infection, although topical corticosteroids and antimicrobials are the first therapeutic choice. The aim of the study was to evaluate the efficacy and safety of an herbal extract of Yunnan Baiyao formulated in toothpaste as an alternative therapy for minor RAS. Yunnan Baiyao is a well-known traditional Chinese medicine, formulated in a powder or capsule form. It was initially and widely used in wounds for its anti-hemorrhagic hemostatic function, and further in gastrointestinal bleeding. Yunnan Baiyao powder has been generally applied on RAS among Chinese population. In this study, a randomized, double-blind, placebo-controlled clinical trial (from March 2010 to March 2011) was conducted on a cohort of 227 minor RAS patients. The toothpaste containing Yunnan Baiyao was used twice daily as part of the patient's routine oral hygiene for 5 days. An assessment of ulcerative size and pain was recorded on Day 0 (baseline), Day 3 and Day 5. Any noted adverse reactions were recorded.

NCT ID: NCT01501409 Completed - Clinical trials for Recurrent Aphthous Stomatitis

Effect of Sodium Lauryl Sulfate on Recurrent Aphthous Stomatitis

Start date: January 2010
Phase: N/A
Study type: Interventional

Sodium lauryl sulfate (SLS) is an anionic detergent that has been used as the major or sole surfactant in most dentifrices. But it is known to local irritating factor to oral mucosa and skin and results in many side effects. This study was to compare the effects of SLS-free dentifrice and SLS-containing dentifrice in patients with recurrent aphthous stomatitis (RAS).

NCT ID: NCT01293968 Completed - Aphthous Stomatitis Clinical Trials

Therapeutic Effects of "Ibuprofen, Diphenhydramine and Aluminium MgS" on Recurrent Aphthous Stomatitis

Start date: November 2010
Phase: Phase 2
Study type: Interventional

The intention of the study is to study the effects of Ibuprofen, Diphenhydramine and Aluminium MgS in decreasing the signs of recurrent aphthous stomatitis (RAS)

NCT ID: NCT01210014 Completed - Aphthous Stomatitis Clinical Trials

Systemic Zinc Sulphate in Treatment of Recurrent Aphthous Ulcerations:A Doubleblind, Placebo Controled Study

Start date: April 2008
Phase: Phase 2
Study type: Interventional

Recurrent aphthous stomatitis (RAS) is one of the most common of oral mucosa diseases that affects approximately 20% of the general population. Despite the fact that clinical, pathologic and therapeutic feature of the disease has been comprehensively studied, the pathophysiology of aphthous ulcers remains incompletely understood. Zinc is a potent catalyst of wound healing and zinc deficiency may be a common cause of delayed tissue repair. Use of zinc sulfate in promotion wound healing and preservation of epithelial integrity advocated its possible use in the treatment or prevention of recurrent oral ulcers. The purpose of the present study was to determine of systemic zinc sulphate in the treatment of recurrent aphthous stomatitis.

NCT ID: NCT01127724 Terminated - Clinical trials for Recurrent Aphthous Stomatitis

Influence of Different Doses of the Vitamin B12 on Recurrent Aphthous Stomatitis

Start date: June 2012
Phase: N/A
Study type: Interventional

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

NCT ID: NCT01122147 Completed - Clinical trials for Recurrent Aphthous Stomatitis

Clinical Evaluation of Fluid Extract of Chamomilla Tincture for Oral Aphthae

Start date: April 2010
Phase: Phase 1
Study type: Interventional

Recurrent aphthous stomatitis is a difficult to treat and quite common chronic inflammatory disease of the oral mucosa. This study evaluates the fluid extract from Chamomilla recutita's safety and effectiveness in treatment of aphthous stomatitis .

NCT ID: NCT00723268 Active, not recruiting - Oral Aphthae Clinical Trials

Evaluation of Therapeutic Effect of 0.5 mg Colchicine and 5 mg Prednisolone on Oral Aphthae

Start date: May 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether low doses of prednisolone, or colchicine are effective in the treatment of oral aphthae.

NCT ID: NCT00556686 Withdrawn - Canker Sore Clinical Trials

Salivary Catecholamines in Aphthous Stomatitis (Canker Sores)

Start date: August 2006
Phase: N/A
Study type: Observational

The purpose of this study is to examine how compounds produced in patients with canker sores affect wound healing.