The effectiveness of russian olive in the treatment of oral aphthae

Phase 3

Recruiting

• Conditions: Oral recurrent aphthous ulcer.; K12.0; Recurrent

• Registration Number: IRCT20150721023282N27
• Lead Sponsor: Esfahan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 6 March 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 34

Inclusion Criteria

Age of 18 years or more
Having 1 to 5 oral aphthous ulcers
No more than 48 hours of aphthous occurrence
Not receiving any systemic antibiotic within the last 2 weeks

Exclusion Criteria

Pregnancy
Lactation
Underlying disease causing oral aphthous ulcer

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Oral aphthous ulcer size. Timepoint: Before the intervention, 2 and 5 days after the start of intervention. Method of measurement: Dental caliper.;Pain severity. Timepoint: Before the intervention, 2 and 5 days after the start of intervention. Method of measurement: Visual Analog Scale.

Secondary Outcome Measures

Name	Time	Method
The number of cases with complete ulcer healing. Timepoint: End of ontervention (5th day). Method of measurement: Observation.