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

Primary Purpose

Recurrent Aphthous Stomatitis

Status
Terminated
Phase
Not Applicable
Locations
Israel
Study Type
Interventional
Intervention
vitamin B12 treatment
Sponsored by
Meir Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Recurrent Aphthous Stomatitis focused on measuring Vitamin B12, Aphthous stomatitis, Cobalamin, Doses

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients aged 18 and older
  • Suffer from RAS For at least one year, with aphthous frequency at least once a month.

Exclusion Criteria:

  • known sensitivity to vitamin B12
  • Don't speak Hebrew, Russian or English.
  • Systemic Diseases, known in developing mouth aphthous (Behcet disease, Lupus Erythematosus, rheumatoid arthritis and AIDS disease)
  • Patients who have received last year any form of vitamin B12 .
  • Patients who receive a different treatment to RAS(not for pain)
  • Pregnant or breastfeeding women
  • patient suffering from Leber's optic atrophy
  • Patients who suffer from Psychosis

Sites / Locations

  • Clalit Health Service (HMO)

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

group 1- 1000 mcg

Group 2- 100 mcg

group 3- 2000 mcg

Arm Description

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 III- will receive sublingual vitamin B12 treatment, 2000 mcg per day for 6 months

Outcomes

Primary Outcome Measures

frequency of recurrent aphthous stomatitis (RAS)

Secondary Outcome Measures

severity of recurrent aphthous stomatitis (RAS)

Full Information

First Posted
May 20, 2010
Last Updated
November 18, 2014
Sponsor
Meir Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT01127724
Brief Title
Influence of Different Doses of the Vitamin B12 on Recurrent Aphthous Stomatitis
Official Title
Influence of Different Doses of the Vitamin B12 on Recurrent Aphthous Stomatitis
Study Type
Interventional

2. Study Status

Record Verification Date
April 2013
Overall Recruitment Status
Terminated
Why Stopped
difficulties in recruiting participants
Study Start Date
June 2012 (undefined)
Primary Completion Date
October 2014 (Actual)
Study Completion Date
October 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Meir Medical Center

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Recurrent Aphthous Stomatitis
Keywords
Vitamin B12, Aphthous stomatitis, Cobalamin, Doses

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
8 (Actual)

8. Arms, Groups, and Interventions

Arm Title
group 1- 1000 mcg
Arm Type
Experimental
Arm Description
Group I- will receive sublingual vitamin B12 treatment, 1000 mcg per day for 6 months
Arm Title
Group 2- 100 mcg
Arm Type
Experimental
Arm Description
Group II- will receive sublingual vitamin B12 treatment, 100 mcg per day for 6 months
Arm Title
group 3- 2000 mcg
Arm Type
Experimental
Arm Description
Group III- will receive sublingual vitamin B12 treatment, 2000 mcg per day for 6 months
Intervention Type
Drug
Intervention Name(s)
vitamin B12 treatment
Other Intervention Name(s)
vitamin B12
Intervention Description
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 III- will receive sublingual vitamin B12 treatment, 2000 mcg per day for 6 months
Primary Outcome Measure Information:
Title
frequency of recurrent aphthous stomatitis (RAS)
Time Frame
12 months
Secondary Outcome Measure Information:
Title
severity of recurrent aphthous stomatitis (RAS)
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients aged 18 and older Suffer from RAS For at least one year, with aphthous frequency at least once a month. Exclusion Criteria: known sensitivity to vitamin B12 Don't speak Hebrew, Russian or English. Systemic Diseases, known in developing mouth aphthous (Behcet disease, Lupus Erythematosus, rheumatoid arthritis and AIDS disease) Patients who have received last year any form of vitamin B12 . Patients who receive a different treatment to RAS(not for pain) Pregnant or breastfeeding women patient suffering from Leber's optic atrophy Patients who suffer from Psychosis
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yan Press, MD
Organizational Affiliation
Ben-Gurion University of the Negev
Official's Role
Principal Investigator
Facility Information:
Facility Name
Clalit Health Service (HMO)
City
Beer-Sheva
Country
Israel

12. IPD Sharing Statement

Learn more about this trial

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

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