Tibolone has been registered for treatment of menopausal symptoms. It is, however, not known
what the effects are of tibolone in postmenopausal women diagnosed with sexual dysfunction.
This is important because there is currently no approved treatment of libido problems in
postmenopausal women. Therefore, the primary aim of this study was to compare the effects of
tibolone with an estrogen/progestogen skin patch in postmenopausal women diagnosed sexual
dysfunction.
Inclusion Criteria:
- Physically and mentally healthy postmenopausal women, >=48 and <=68 years of age,
with an intact uterus.
- Women were to suffer from decreased satisfactory sexual activity compared to younger
age and sexual problems were not to be considered caused by relationship/partner
problems. The decreased sexual functioning was to result in sexually related personal
distress as confirmed by the FSDS (score =15).
- An affirmative answer was to be given to the following questions: (a) In previous
years did you find sexual activity satisfying? (b) Has there been a decline in your
satisfaction with sexual activity? (c) Are you satisfied with your partner as a
friend?
- All subjects were to have an established sexual relationship of at least 6 months
duration prior to screening.
- Women were to be sexually active.
- Normal mammography within 6 months prior to randomization.
- Body mass index >18 and <=32 kg/m2.
- Voluntary written informed consent
Exclusion Criteria:
- Any unexplained abnormal uterine bleeding
- Double layer endometrial thickness >4 mm
- Tibolone or transdermal E2/NETA use within 3 months prior to screening
- Progestogen implants or injections and estrogen/progestogen injectable therapy within
6 months prior to screening
- Use of intra-uterine progestogen
- Unsuccessful previous treatment with androgens or compounds known to enhance
androgenic activity
- Current successful treatment with androgens, without applying the applicable washout
period of 3 months prior to screening
- Any previous or current unopposed estrogen administration, prior use of estrogen
pellets or tamoxifen citrate (previous low dose vaginal estrogen-only applications
are allowed)
- Use of anti -androgens within the preceding 5 years prior to screening.
- Women with significant organic disorder of sexual dysfunction or a partner with
sexual dysfunction
- Women who had early onset sexual dysfunction (>15 years prior to menopause)
- Women suffering from androgenic alopecia, acne or hirsutism
- Women suffering from illnesses influencing sexuality
- Women using medication influencing sexuality
- Moderate to severe depression
- Current or prior use of antidepressant within 8 weeks prior to screening
- Major gynecological surgery in the preceding 3 months
- Any serious disease or disorder; or any endocrine disorder with systemic disease
which would have impaired overall health and well being (controlled
hypo/hyperthyroidism and diabetes mellitus Type II was allowed)
- History or presence of severe psychiatric illness and/or any addictions to drugs,
medication or alcohol in the past 3 years
- Diseases for which exogenous hormonal steroids were contraindicated.
- History or presence of any malignancy, except successfully treated non-melanoma skin
cancers
- History or presence of cardiovascular or cerebrovascular conditions, thrombosis or
thromboembolic disorders
- History or presence of liver, gallbladder or renal disease, epilepsy or classical
migraine headaches
- Uncontrolled hypertension
- Women with abnormal cervical smear results
- History or presence of breast cancer, suspicious breast lump or mammographic
abnormality
- Known hypersensitivity to any of the ingredients of the trial medication.
- Non-compliance with the screening diary
- Current use of raloxifene, clonidine, veralipride, phytoestrogen extracts
- Drugs known to interfere with the pharmacokinetics of the steroids
- Use of investigational drugs within the past 60 days
- Any disease or condition that was clinically relevant and which, in the opinion of
the investigator, would have jeopardized the subject's well being during the course
of the trial
