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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00527306
Other study ID # 06-022-1
Secondary ID DF 04-005
Status Completed
Phase Phase 3
First received
Last updated
Start date December 2005
Est. completion date July 2009

Study information

Verified date August 2020
Source UConn Health
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this research study is to find out if taking a multivitamin daily can affect the number of canker sores that people get and how long they last. Previous studies have shown that people who get canker sores are more likely to be deficient in one or more vitamins. It has also been found that correction of such vitamin deficiencies reduces the number and duration of canker sores. However, it is not known if taking a multivitamin daily will reduce the number and duration of canker sores.


Recruitment information / eligibility

Status Completed
Enrollment 160
Est. completion date July 2009
Est. primary completion date July 2009
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients willing and able to provide written informed consent for the study

- Patients with a history of at least three episodes of minor recurrent aphthous stomatitis (RAS) within the past one year

Exclusion Criteria:

- Patients with a history of other forms of RAS (major, herpetiform)

- Patients who will be using any other vitamins/supplements during the study or those who have used any vitamins/supplements on a regular basis during the 90 days immediately preceding enrollment onto the study (regular use is defined as continuous daily use for at least a two week period)

- Patients who are under the age of 18

- Women who are pregnant or nursing or those who plan to become pregnant

- Patients with a history of gout, kidney stones or iron overload disease

- Patients who currently smoke tobacco products

- Patients who are former smokers who have quit smoking within the past 30 days

- Patients with sulfite allergy

- Patients with a history of any systemic condition associated with oral ulceration. These include: Behcet's syndrome, Sweet's syndrome, Celiac disease, Crohn's disease, ulcerative colitis, HIV infection/AIDS, cyclic neutropenia and PFAPA syndrome (periodic fever, aphthous stomatitis, pharyngitis and cervical adenitis)

- Patients on medications commonly associated with causing oral ulceration. These include nicorandil, methotrexate and chemotherapeutic agents used for cancer.

- Patients using oral topical anti-inflammatory agents during the course of the study

- Patients who plan to use any products specifically for management of RAS lesions

- Patients who are routinely using agents that could have an impact on duration of RAS lesions (e.g., antibacterial mouthrinses)

- Patients receiving any other investigational agent during the course of ths study

- Patients with any other condition that might preclude participation in the study in the opinion of the study investigators

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
multivitamin
Subject will be asked to take a multivitamin capsule or a placebo (inactive pill) once a day for one year. There will be an equal chance of getting the multivitamin or the placebo.

Locations

Country Name City State
United States University of Connecticut Health Center Farmington Connecticut

Sponsors (2)

Lead Sponsor Collaborator
UConn Health Donaghue Medical Research Foundation

Country where clinical trial is conducted

United States, 

References & Publications (3)

Huling LB, Baccaglini L, Choquette L, Feinn RS, Lalla RV. Effect of stressful life events on the onset and duration of recurrent aphthous stomatitis. J Oral Pathol Med. 2012 Feb;41(2):149-52. doi: 10.1111/j.1600-0714.2011.01102.x. Epub 2011 Nov 12. — View Citation

Kozlak ST, Walsh SJ, Lalla RV. Reduced dietary intake of vitamin B12 and folate in patients with recurrent aphthous stomatitis. J Oral Pathol Med. 2010 May;39(5):420-3. doi: 10.1111/j.1600-0714.2009.00867.x. Epub 2010 Feb 7. — View Citation

Lalla RV, Choquette LE, Feinn RS, Zawistowski H, Latortue MC, Kelly ET, Baccaglini L. Multivitamin therapy for recurrent aphthous stomatitis: a randomized, double-masked, placebo-controlled trial. J Am Dent Assoc. 2012 Apr;143(4):370-6. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Annual number and average duration of minor recurrent aphthous stomatitis (canker sores) episodes one year
Secondary Pain due to recurrent aphthous stomatitis (canker sores); impact of recurrent aphthous stomatitis on ability to consume a normal diet one year
See also
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Completed NCT04884464 - Hyaluronic Acid in Counteracting Aphthous Stomatitis
Withdrawn NCT02535962 - Probiotics and Corticosteroids for Treating Periodic Fever, Aphthous Stomatitis, Pharyngitis, Cervical Adenitis (PFAPA) Phase 2
Completed NCT01293968 - Therapeutic Effects of "Ibuprofen, Diphenhydramine and Aluminium MgS" on Recurrent Aphthous Stomatitis Phase 2
Completed NCT04677062 - Safety, Galenic Acceptability and Efficacy of GV-328 Lozenges in Children With Oral Aphthosis N/A
Completed NCT02890524 - Tokushima Night Guard for Recurrent Aphthous Stomatitis N/A
Completed NCT02789605 - Effectiveness and Safety of Lactobacillus Rhamnosus Lcr35® in the Treatment of Recurrent Aphthous Stomatitis Phase 2
Recruiting NCT05772338 - Efficacy and Safety of BNP105 in the Treatment of Recurrent Aphthous Stomatitis N/A
Completed NCT00001601 - Evaluation and Treatment of Oral Soft Tissue Diseases N/A
Completed NCT01210014 - Systemic Zinc Sulphate in Treatment of Recurrent Aphthous Ulcerations:A Doubleblind, Placebo Controled Study Phase 2