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Investigating the effect of burn wound healing spray.

Phase 2
Recruiting
Conditions
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Burn of unspecified body region, unspecified degree
T30.0
Registration Number
IRCT20240309061227N1
Lead Sponsor
Hamedan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
40
Inclusion Criteria

Age group 10 to 70 years
Having first and second-degree burns, at least one square centimeter of the skin surface
Fully alert and able to understand instructions and self-care (including not rubbing, touching and scratching the burn site)

Exclusion Criteria

History of allergy to herbal medicines
History of asthma, COPD, hay fever, skin allergy
Use of anti-inflammatory drugs (glucocorticosteroids, NSAIDs) in the last three months
The presence of a skin lesion that prevents the examination of burns
Diabetic patients with diabetic ulcers
Concurrent participation in at least one other clinical trial affecting burns

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Recovery percentage. Timepoint: daily during the entire study period. Method of measurement: Recovery percentage will be calculated using the formula.;Duration of treatment with herbal formulation. Timepoint: Daily. Method of measurement: The time interval between the start of treatment and recovery.
Secondary Outcome Measures
NameTimeMethod
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