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Evaluation of the efficacy of Alum in wound size of oral Aphthous

Evaluation of the efficacy of Alum mucosal adherent in management of wound size of Recurrent Aphthous Stomatitis in Hamadan dental faculty in comparison with placebo group

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201305275678N2
Enrollment
50
Registered
2014-06-12
Start date
2013-03-20
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

recurrent aphtous stomatitis. Recurrent oral aphthae

Interventions

Case group:"Aplication of mucous Adhesives containing alum" Control group: "Application ofadhesive without alum(placebo) ".
Treatment - Drugs
Case group:"Aplication of mucous Adhesives containing alum" Control group: "Application ofadhesive without alum(placebo) "

Sponsors

research center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 30 Years

Inclusion criteria

Inclusion criteria: Criteria for inclusion : people (male or female) over 15 years,The patient had a history of aphtous (at least 3 times a year), have a lesion less than 10 mm diameter,This ulcer must be in the areas of the mouth, which can be easily used in medicine including the tongue, floor of the mouth and the lining of the cheek Mucosa, lbial. should be a maximum of 3 days begining of new lesions (new lesion) ,no history of tratment Exclusion criterias:pregnancy or lactating subjects ,patients with systemic diseases associated withAphtous like Cron,Rhiter and Behcet's disease ,consumption of chewable tobacco or cigarettes and ,Viral and fungal diseases , treatment with any other drug, consumption of acetaminophen and NSAID'S orantihistamine or another medication to treat thelesions, oral surgery over the past two weeks , orthodontic wire and bracket or restorative treatment

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
The size of the wound. Timepoint: days1,3,5. Method of measurement: ruler.

Secondary

MeasureTime frame
The intensity of the pain. Timepoint: days 1,3,5. Method of measurement: visual analogue scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Shahrbanou Raedi

dental faculty-departmant of oral medicine

dr.radi80@yahoo.com+98 81 1835 4016

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026