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The pilot study was designed as a self-control medical trial. Clients with post-mastectomy lymphedema had been recruited. A double-herb formulation ( ) with standard dose had been administered orally in a powdered type, 6 times each week for six months. Outcome measurements included standard limb volume modifications assessed by liquid displacement method; handgrip strength; and QOL for limb lymphedema questionnaire (LYMQOL). There were n