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Comparison of Aaftin gel with Triamcinolone effect in patient with Aphthous ulcer

Phase 3
Recruiting
Conditions
Aphthous Ulcer.
Recurrent oral aphthae
Registration Number
IRCT20180707040375N1
Lead Sponsor
Sohrab sarhadi (myself)
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
40
Inclusion Criteria

Avoid patients with systemic disease

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The amount of pain and irritation. Timepoint: Before the intervention, 2 hours after the intervention, the second day, the fourth day, the sixth day. Method of measurement: VAS scale.
Secondary Outcome Measures
NameTimeMethod
Size of the wound. Timepoint: Before the intervention, 2 hours after the intervention, the second day, the fourth day, the sixth day. Method of measurement: Graph paper.
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