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probiotic on oral aphtus ulcers

Evaluation of therapeutic effect of pro biotic medication on oral recurrent aphtus ulcers

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20110428006322N2
Enrollment
40
Registered
2019-10-17
Start date
2019-07-23
Completion date
Unknown
Last updated
2019-11-05

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

Conditions

oral recurrent aphtus ulcer. Stomatitis and related lesions

Interventions

Intervention 1: Intervention group: Treatment with probiotic product or probiotic products from Lactobacillus routeri is administered in a gel-sol form, which patients put in the mouth on the lesion a

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: patients with oral aphtus ulcers between 15 -80 years old. patients with oral aphtus ulcers without any systemic medication during last 6 months. patients with one to three oral aphtus ulcers in their mouths Patients with oral lesions that do not have a day off at the beginning of the lesion (the lesion is on the first day of appearance) Patients with oral lesions that do not have a history of rheumatologic disease, GI disease, renal disease, and iron deficiency anemia.

Exclusion criteria

Exclusion criteria: Patients with oral aphtus lesions that have had a lesion more than one day. pregnant patients Patients with diffuse oral lesions and more than 3 concurrent lesions Patients who do not have the opportunity to travel for frequent or repeated examinations.

Design outcomes

Primary

MeasureTime frame
The size of the lesions in millimeters. Timepoint: determination at 1,3,5 and 7 days. Method of measurement: size determination by ruler.;Severity of burning and pain based on visual analogue score (VAS) (score between 0-10). Timepoint: determination at 1,3,5 and 7 days. Method of measurement: Evaluation by VAS method and numerical expression of pain and burning intensity.;Duration of recovery in terms of number of days. Timepoint: daily check for seven days. Method of measurement: Improvement of clinical symptoms, absence of oral lesions and complete relief of burning and pain.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMostafa Rezaee

Shiraz University of Medical Sciences

rezaim@sums.ac.ir+98 71 3628 9917

Outcome results

None listed

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