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Preparation and clinical evaluation of a aloe vera and thymol buccal gel for the treatment of aphthous stomatitis

Preparation and clinical evaluation of a aloe vera and thymol buccal gel for the treatment of aphthous stomatitis: An experimental study and a double blinded randomized clinical trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20191106045356N9
Enrollment
50
Registered
2021-11-20
Start date
2022-04-03
Completion date
Unknown
Last updated
2022-03-08

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

Conditions

Aphthous stomatitis. Recurrent oral aphthae

Interventions

Intervention 1: Intervention group: Patients will use 7% of pentoxifylline adhesive mucus gel prepared at Shahid Sadoughi School of Pharmacy in Yazd twice a day at the rate of one drop per lesion. At

Sponsors

Yazd University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients with aphthous stomatitis starting up to two days No pregnancy and lactation Patients between 18_65 years old No history of allergies to aloe vera and thymol

Exclusion criteria

Exclusion criteria: Patients with skin diseases Sensitivity to aloe vera and thyoml or any of components of the product Do not use the drug for two consecutive days Exacerbation of the aphthous stomatitis

Design outcomes

Primary

MeasureTime frame
Severity of pain. Timepoint: At the beginning of treatment and after every 2 to 10 days, the condition of aphthous lesions is evaluated for pain intensity (score 0 to 4). Method of measurement: Scoring pain using a questionnaire.

Secondary

MeasureTime frame
Redness and inflammation. Timepoint: At the beginning of treatment and after every 2 to 10 days, the condition of aphthous lesions is evaluated for the severity of redness and inflammation (score 0 to 4). Method of measurement: Scoring severe redness and inflammation using a questionnaire.;Total area of ??aphthous lesions. Timepoint: At the beginning of treatment and after every 2 to 10 days, the condition of the aphthous lesions is evaluated in terms of the total area of ??the aphthous lesions. Method of measurement: Determining the total area of ??aphthous lesions through Fiji software.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Mohsen Zabihi

Yazd University of Medical Sciences

mzabihi100@gmail.com+98 35 3820 3865

Outcome results

None listed

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