Subjects
The authors recruited 36 healthy, adult volunteers
with no underlying skin disease or skin lesion on
the test area. All subjects were older than 15 years old,
non-pregnant, and not breastfeeding. Patients with a
history of allergies or with known allergy to the test
products and patients receiving immunosuppressive
therapy, corticosteroids, antihistamines, and/or chemotherapy
in the previous two weeks were excluded. The
volunteers must be able to attend all four days of the
test period and must be able to comply with the restrictions
during the test period, which included to not
participate in any activity or exercise that will cause
sweating and to keep the test area dry until the last
reading. All volunteers were informed of objectives,
test procedures, and possible adverse effects, and
were rewarded for their time of participation. They were
included into the present study only after signing the
consent form.
The volunteers recruited were females aged
between 20-60 years (mean age 35.8). Three of the
volunteers were taking other medications that were
considered not to interfere with the present study
including antihypertensive drugs, thyroid hormone,
and oral contraceptive pills.
Subjects
The authors recruited 36 healthy, adult volunteers
with no underlying skin disease or skin lesion on
the test area. All subjects were older than 15 years old,
non-pregnant, and not breastfeeding. Patients with a
history of allergies or with known allergy to the test
products and patients receiving immunosuppressive
therapy, corticosteroids, antihistamines, and/or chemotherapy
in the previous two weeks were excluded. The
volunteers must be able to attend all four days of the
test period and must be able to comply with the restrictions
during the test period, which included to not
participate in any activity or exercise that will cause
sweating and to keep the test area dry until the last
reading. All volunteers were informed of objectives,
test procedures, and possible adverse effects, and
were rewarded for their time of participation. They were
included into the present study only after signing the
consent form.
The volunteers recruited were females aged
between 20-60 years (mean age 35.8). Three of the
volunteers were taking other medications that were
considered not to interfere with the present study
including antihypertensive drugs, thyroid hormone,
and oral contraceptive pills.
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