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Cecilia Lundin
Cecilia Lundin
Department of Women’s and Children’s Health, Uppsala University, Uppsala, Sweden
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Agota Malmborg
Agota Malmborg
Obstetrics and Gynaecology, Department of Clinical and Experimental Medicine, Linköping University, Linköping, Sweden
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Julia Slezak
Julia Slezak
Clinical Chemistry, Department of Clinical and Experimental Medicine, Linköping University, Linköping, Sweden
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Kristina Gemzell Danielsson
Kristina Gemzell Danielsson
Department of Women’s and Children’s Health, Karolinska Institutet, and Karolinska University Hospital, Stockholm, Sweden
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Marie Bixo
Marie Bixo
Department of Clinical Science, Obstetrics and Gynaecology, Umeå University, Umeå, Sweden
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Hanna Bengtsdotter
Hanna Bengtsdotter
Department of Obstetrics and Gynaecology, Örebro University, Örebro, Sweden
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Lena Marions
Lena Marions
Department of Clinical Science and Education, Karolinska Institutet Södersjukhuset, Stockholm, Sweden
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Ingela Lindh
Ingela Lindh
Department of Obstetrics and Gynaecology, Sahlgrenska Academy at Gothenburg University, Sahlgrenska University Hospital, Gothenburg, Sweden
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Elvar Theodorsson
Elvar Theodorsson
Clinical Chemistry, Department of Clinical and Experimental Medicine, Linköping University, Linköping, Sweden
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Mats Hammar
Mats Hammar
Obstetrics and Gynaecology, Department of Clinical and Experimental Medicine, Linköping University, Linköping, Sweden
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Inger Sundström-Poromaa
Inger Sundström-Poromaa
Department of Women’s and Children’s Health, Uppsala University, Uppsala, Sweden
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with a COC (1.5 mg oestradiol and 2.5 mg nomegestrol acetate) or placebo during three 24/4 treatment cycles. During the screening visit blood and hair samples were collected and women filled out the McCoy Female Sexuality Questionnaire (MFSQ) ( 15
