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Comparing the effect of Verapamil and triamcinolon in Hypertrophic scar treatment

Phase 2
Conditions
Hypertrophic scar.
Keloid scar
Registration Number
IRCT2016010425539N5
Lead Sponsor
Vice chancellor for research, Iran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
50
Inclusion Criteria

Patients with hypertrophic scar and keloid which had not any other treatment and after accept of survey condition to come montly for enjection.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Hypertrophic scar. Timepoint: The month 0, 1, 2 during treatment and 1 month after treatment. Method of measurement: The highest elevation of hypertrophic scar with calliper and ruler.
Secondary Outcome Measures
NameTimeMethod
Patient satisfaction from treatment. Timepoint: After treatment. Method of measurement: The percentage and score of the patient to treatment.
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