The purpose of this study is to compare combined postmenopausal hormone therapy natural progesterone to the one containing synthetic progestagen (i.e. chlormadinone acetate) at the blood transcriptome level.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Masking
NONE
Enrollment
40
200 mg/day oral micronized natural progesterone (e.g. Utrogestan® 100mg) + 0.05 mg/day transdermal (i.e. plaster) 17β-estradiol (e.g. Estraderm® 50µg) during a year
5 mg/day oral chlormadinone acetate (e.g. Luteran® 5mg)+ 0.05 mg/day transdermal (i.e. plaster) 17β-estradiol (e.g. Estraderm® 50µg)
Gynecology center, Helse Nord
Bodø, Norway
Whole blood and white blood cells gene expression profiling after 3 months of HT treatment
Time frame: 0 and 3 months after treatment
Quality of life, proteome, plasma haemostatic variable measurements
Time frame: 0,3,6 and 12 months
Whole blood and white blood cells gene expression profiling after 12 months of HT treatment
Time frame: 0 and 12 months after treatment
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