The purpose of this study is to evaluate the effects on breast in postmenopausal women randomized to either oestradiol in combination with DRSP or E2 in combination with NETA during six months.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
120
1 mg of oral oestradiol (E2) in continuous combination with 2 mg of DRSP or 1 mg of oral E2 in continuous combination with 0.5 mg of NETA during six months.
Karolinska University Hospital
Stockholm, Sweden
RECRUITINGMammographic breast density - classified according to digitized data-based quantification of breast density.
Time frame: 6 months
Effects on serum levels of Oestradiol etc.
Time frame: 6 months
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