MedPath

Efficacy of oral safflower oil in treatment of melasma

Phase 3
Recruiting
Conditions
Melasma.
Chloasma
L81.1
Registration Number
IRCT20150825023753N15
Lead Sponsor
Shiraz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
40
Inclusion Criteria

Diagnosis of melasma by a dermatologist
The patient is bound to cooperate for regular use of the studied drug and refer at the appointed time
Having informed and written consent to participate in the study
Satisfaction with not using out-of-protocol therapies

Exclusion Criteria

Pregnant and lactating women
Individuals with other organ disorders (cancers, liver, kidney)
History of hypersensitivity reaction to safflower seeds
39/5000Patient dissatisfaction to continue the project for any reason
Individuals with diabetes
Taking skin lightening medications in the last two weeks
Taking hormonal contraceptives and other medications that cause melasma
Taking anticoagulants (aspirin, Plavix, warfarin)
Individuals with coagulation diseases
History of hypersensitivity to safflower seeds

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The rate of melasma discoloration. Timepoint: Measurements are taken at the start of the study, one month and two months after the start of the study. Method of measurement: Using Visioface 1000D and The Melasma Area and Severity Index (MASI).
Secondary Outcome Measures
NameTimeMethod
Quality of life of patients with melasma. Timepoint: This variable is measured at the beginning of the study and two months later. Method of measurement: The Melasma Quality of Life scale (MELASQOL).
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