This study is conducted in Europe. The aim of this study is to investigate the bleeding profile after switch from Trisekvens® to Activelle® (1.0 mg estradiol / 0.5 mg norethisterone acetate (NETA)).
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
191
After a screening period of 12 weeks (three lunar months) in which the subjects still are on Trisekvens® followed by a treatment period of 24 weeks (six lunar months) in which the subjects are treated with Activelle®.
Novo Nordisk Investigational Site
Kristiansand, Norway
Novo Nordisk Investigational Site
Kristiansund, Norway
Postmenopausal women's acceptance of bleeding
Time frame: After 24 weeks of treatment
Bleeding profile in postmenopausal women
Time frame: After 24 weeks of treatment
Acceptance of hot flushes and breast tenderness
Time frame: After 24 weeks of treatment
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Novo Nordisk Investigational Site
Larvik, Norway
Novo Nordisk Investigational Site
Oslo, Norway
Novo Nordisk Investigational Site
Trondheim, Norway
Novo Nordisk Investigational Site
Borås, Sweden
Novo Nordisk Investigational Site
Gothenburg, Sweden
Novo Nordisk Investigational Site
Gothenburg, Sweden
Novo Nordisk Investigational Site
Kungsbacka, Sweden
Novo Nordisk Investigational Site
Linköping, Sweden
...and 9 more locations