Eczema Clinical Trial
Official title:
Product Functional Study of Effect A Master Ganoderma Detox Tea on Eczema Patient
This is a single-blind, cross-over pilot study to observe the safety and efficacy of Ganoderma tea on eczema patients.
Objective This study is to conduct a preliminary observation on the effect of A Master
Ganoderma Detox Tea in improving eczema symptoms. Because it is a preliminary study, there
will not be a placebo control. However, in order to exclude the impact of spontaneous
improvement, we will set up a cross over control group. Thus, we want to find out whether
there is any difference in taking the tea and without taking the tea.
Research Design This is a randomized, cross-over-control and assessor-blinded clinical
trial. Subjects will be divided into groups A and group B. Group A will receive the
intervention for 8 weeks, followed by an 8-week period of no intervention. Group B will be
observed without having any intervention for 8 weeks, and then receive the intervention for
8 weeks. Randomization will be carried out using a computer program.
Interventions Subjects in the treatment group (A) will take the A Master Ganoderma Detox Tea
for 8 weeks. Initially, the dosage is twice a day, one pack (5g) each time, and then
increased to three times a day, two packs each time within two weeks. The control group (B)
will not receive any study intervention for 8 weeks, followed by similar intervention for 8
weeks.
In case of allergies or severe adverse reactions occur, the subject should stop taking the
tea immediately and be excluded from the trial. During the control or intervention period,
if necessary, subject may use short-term steroids or other topical medication to relieve the
symptoms of eczema.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment
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