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Comparison of effectiveness of the Bioadhesive paste Containing Licorice 5% with Bioadhesive Paste without drug in the Management of Recurrent Aphthous Stomatitis

Comparison of effectiveness of the Bioadhesive paste Containing Licorice 5% with Bioadhesive Paste without drug in the Management of Recurrent Aphthous Stomatitis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201011273133N2
Enrollment
60
Registered
2011-01-31
Start date
2010-06-04
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 aphthous stomatitis. recurrent aphthous stomatitis

Interventions

Intervention 1: Intervention group: Bioadhesive paste Containing Licorice 5% 4 times per days 1h before meal and 20 minutes before sleep. Intervention 2: Control group: diphen hydramin elixir, 5 cc, 4
Treatment - Drugs
Intervention group: Bioadhesive paste Containing Licorice 5% 4 times per days 1h before meal and 20 minutes before sleep
Control group: diphen hydramin elixir, 5 cc, 4 times per days 1h before meal and 20 minute before sleep
Control group: Bioadhesive paste without Licorice 5%, 4 times per days 1h before meal and 20 minute before sleep

Sponsors

Zahedan University of Medical Siences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: history of recurrent aphthous stomatitis, Current suffering from ulceration in 1 day, signed a well-explained written informed consent form Exclusion criteria: Pregnancy, lactation (Urine hCG-positive), Ulcers as a manifestation of a systemic disease process such as ulcerative colitis, Crohn's disease, Behcet's syndrome, serious anemia, treatment with systemic steroid or other immunomodulatory agents within 1 month before the study entry, ulcer in tongue, major RAS, presenting with more 1 aphthous ulcers, after 24 hours' duration of ulcer

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Diameter of the lesion with erythematois rim. Timepoint: 48 hours. Method of measurement: periodental prob.;Diameter of necrotic zone. Timepoint: 48 hours. Method of measurement: periodental prob.;Pain level. Timepoint: 48 hours. Method of measurement: visual analoge scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNarjes Akbare

Zahedan University of Medical Sciences,

narges_akbare4021@yahoo.com+98 54 1243 1289

Outcome results

None listed

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