Efficacy and Safety of Oral DHEA Therapy for Postmenopausal Women on Sexual Function, Wellbeing and Vasomotor Symptoms

Quality of Life Clinical Trial

Official title: A Randomised, Double-blind, Placebo-controlled, Parallel-group, 52-week Study to Evaluate the Efficacy and Safety of Oral DHEA Therapy for Postmenopausal Women on Sexual Function, Wellbeing and Vasomotor Symptoms

Status Completed

Clinical Trial Summary

This study is designed to evaluate the efficacy and safety of oral Dehydroepiandrosterone (DHEA) 50mg daily, for 12 months in naturally menopausal women with low libido who are not receiving systemic oestrogen or oestrogen- progestin therapy.

Efficacy measures for the present study are effects on sexual function, wellbeing and menopausal symptoms. Safety measures will include endometrial assessment by transvaginal ultrasound (TVU), vital signs, lipid profiles, general electrolytes, effects on glucose metabolism and reports of adverse events.

Clinical Trial Description

Dehydroepiandrosterone (DHEA) and its sulphate (DHEAS) are the most abundant sex steroids in women. Dehydroepiandrosterone sulphate (DHEAS), a unique secretory product of the adrenal gland, and DHEA are converted at various sites in the body, such as the brain, bone and adipose tissue to estrogen or testosterone and their various by-products. DHEAS and DHEA levels decline with age and there has been considerable conjecture that this results in a loss of well-being and libido. DHEA is available as an over-the-counter nutritional supplement in the United States, and is being increasingly prescribed and formulated by compounding pharmacies across Australia. However, there is a paucity of data regarding the effects of oral DHEA on the well-being, sexual function and safety in women. Previous studies evaluating the effects of DHEA on either postmenopausal women or women with adrenal deficiency (Addison's disease) have produced conflicting results, with some studies finding benefit in terms of sexual function and well-being while other studies have found no benefit. Therefore, there is a need for an appropriately powered randomized controlled trial of the effects of DHEA therapy on sexual function and well-being in postmenopausal women. In addition, as DHEA may be metabolized to estrogens, whether DHEA will alleviate vasomotor symptoms merits evaluation. The effects of DHEA on the endometrial (uterine) lining requires assessment, given its potential to be converted to estrogen.

The primary aim of the current study will be to assess the effects of DHEA therapy in naturally menopausal women on sexual function using the Sabbatsberg Self-Rating Scale (SSS) over 12 months in a randomized placebo controlled trial. In addition the effects on well-being will be assessed by the Psychological General Well-Being (PGWB) Index and menopausal symptoms will be evaluated by the Menopause Quality of Life (MENQOL) Intervention Questionnaire. A diary record will also be employed to assess the effects on sexual function. Safety will be assessed over the entire study. Participants will also undergo a transvaginal ultrasound (TVU) at the beginning and end of the study, to determine whether DHEA affects the endometrial lining.

This randomized, double-blind, placebo-controlled study will be conducted in 240 women over a 52-week period. Women will be randomized to receive either placebo or DHEA (50 mg/day) for a 52-week period. It is anticipated that the study will require a 6-month recruitment period. The study duration will be approximately 56 weeks, with a 4-week screening period and treatment period of 52 weeks. The study will be conducted over approximately 13 months. This is a single-centre study and will be conducted at the Alfred Hospital.

Potential participants will be generally healthy women aged 40 - 65 years who have undergone a natural menopause and are in a stable monogamous sexual relationship and not using hormone therapy (HT).

Participants are required to attend 6 clinic visits over a blinded treatment period of 52 weeks. Informed consent will be obtained from the participant prior to the commencement of any study procedure at the first clinic visit. If participants are eligible, they will be asked to return at the end of the screening period to be randomized and commence treatment. During the treatment period, participants will take one capsule daily (placebo or DHEA 50 mg). All participants will return to the clinic 5 more times, at weeks 0, 12, 26, 38 and 52 for assessments of efficacy and safety. Blood tests will be collected at Weeks -4, 0, 12, 26 and 52 to assess safety and hormone levels. Prior to commencing the study, participants will require a mammogram if this has not been done within 12 months of study entry. A transvaginal ultrasound will be performed to assess endometrial thickness prior to commencement of the trial. A Papanicolaou smear will also be performed if the cervix is still present, in those women where a Pap smear has not been done within 12 months of screening. These investigations, except the mammogram and Pap smear, will be repeated at the completion of the study. All participants will have a complete physical examination which will include an assessment of vital signs, breast examination, and internal and external pelvic examination to assess for clitoromegaly (clitoral enlargement). Skin evaluations for scalp hair loss, hirsutism and acne, and assessment for voice changes will be made throughout the study. Participants will be required to complete various questionnaires to assess sexual function (SSS), menopausal symptoms (MENQUOL Intervention) and general well-being (PGWB) at Weeks 0, 12, 26 and 52. Participants will also record satisfactory sexual events in a 28 day diary which will be done in the 4 weeks prior to Weeks 0, 12, 26 and 52. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Libido Disorder
• Menopausal Syndrome
• Quality of Life

• NCT number: NCT00289926
• Study type: Interventional
• Source: Monash University
• Status: Completed
• Phase: Phase 3
• Start date: February 2006
• Completion date: April 2008