Efficacy and Safety of Oral Dehydroepiandrosterone as a Concomitant Therapy to Oral Contraceptives in Women Complaining of Reduced Libido

Phase 2

Completed

• Conditions: Libido
• Interventions: Drug: Dehydroepiandrosterone, BAY86-5314; Drug: Placebo

• Registration Number: NCT00566384
• Lead Sponsor: Bayer

Brief Summary

The purpose of the study is to evaluate the effectiveness of the study drug on the libido (sexual desire) of women who are taking oral contraceptives and who have experienced libido reductions as a side-effect of this contraceptive method The hypothesis is that there is superiority in the change in sexual desire and arousal component scores of the FSFI questionnaire from baseline to cycle 6 of the treatment with the study drug as compared to Placebo.

Detailed Description

Not available

Study Timeline

• Study Start: 2007-11
• Study First Submitted: 2007-11-29
• Study First Submitted QC: 2007-11-30
• Study First Posted: 2007-12-03
• Primary Completion: 2009-04
• Study Completion: 2009-04
• Status Verified: 2014-11
• Last Update Submitted: 2014-11-30
• Last Update Posted: 2014-12-02

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 100

Inclusion Criteria

• Treatment with a oral contraceptive (OC) for at least 3 months and willing to continue the OC
• Loss of libido
• Sexual relationship with a sexually competent partner

Exclusion Criteria

• Female sexual dysfunction other than HSDD, arousal and orgasmic disorder, such as sexual aversion/phobic disorder, sexual pain disorder/dyspareunia

• Hyperandrogenemic conditions, such as congenital adrenal hyperplasia (CAH), polycystic ovary syndrome (PCOS), Cushing's syndrome or signs of hyperandrogenism like severe hirsutism or severe acne

• Presence or a history of venous or arterial thrombotic/thromboembolic events (e.g., deep venous thrombosis, pulmonary embolism, myocardial infarction) or of a cerebrovascular accident.

• Presence or history of prodromi of a thrombosis (e.g., transient ischaemic attack, angina pectoris).

• History of migraine with focal neurological symptoms.

• Diabetes mellitus with vascular involvement.

• Presence of a severe or multiple risk factor(s) for venous or arterial thrombosis

• Pancreatitis or a history thereof if associated with severe hypertriglyceridemia

• Presence or history of severe hepatic disease as long as liver function values have not returned to normal.

• Presence or history of liver tumors (benign or malignant).

• Known or suspected sex-steroid influenced malignancies (e.g., of the genital organs or the breasts)

• Undiagnosed vaginal bleeding.

• Known or suspected pregnancy.

• Hypersensitivity to the active substances or to any of the excipients.

• Body-mass index (BMI ) more than 30.0 kg/m²

• Hypersensitivity to any of the study drug ingredients

• Any disease or condition that can compromise the function of the body systems and could result in altered absorption, excessive accumulation, impaired metabolism, or altered excretion of the study medication

• Known current or history of alcohol or drug abuse

• Prohibited concomitant medication:

  • Use of additional steroid hormones, anticoagulants (e.g., heparin, coumarin), antiepileptics (hydantoin derivates, e.g., phenytoin or carboxamide derivates, e.g., carbamazepin, oxcarbamazepin), other antiepileptics, (e.g., Felbamate, Topiramate), hypnotic and sedative (e.g., barbiturate derivates, primidone), tuberculostatics (e.g., rifampicin), oral antimycotics (e.g., griseofulvin, ketoconazole, itraconazole, fluconazol), virostatic agents (e.g., ritonavir), and products containing St. John's wort and continuous systemic use of antibiotics.
  • Medication with influence on libido (e.g., antihypertensives like beta-adrenergic blocker, cholinesterase blocking agents), psychotropic drugs (e.g., antidepressants, neuroleptic agents, selective serotonin reuptake inhibitors [SSRIs]), lipid lowering drugs and H2 blockers.

• Intake of an experimental drug within 3 months prior to inclusion in the study

• Previous assignment to treatment (e.g., randomization) during this study

• Close affiliation with the investigational site; e.g., a close relative of the investigator, dependent person (e.g., employee or student of the investigational site).

• Operation scheduled in the study period

• Abnormal laboratory values within the non-inclusion range

• Patient is in custody by order of an authority or a court of law

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Arm 1	Dehydroepiandrosterone, BAY86-5314	-
Arm 2	Placebo	-

Primary Outcome Measures

Name	Time	Method
FSDS questionnaire (sexual desire and arousal component scores)	at baseline and after Cycle 6

Secondary Outcome Measures

Name	Time	Method
Serum hormone levels (SHBG, T, DHEA, DHEA-S)	Cycle 1, 3, 6 and follow-up
FSDS-R questionnaire results	Cycle 1, 3, 6 and follow-up
Change from baseline period to cycle 6 in the number of satisfactory sexual events	after Cycle 6
FSFI questionnaire (absolute values and change from baseline) - All domains	Cycle 1, 3, 6 and follow-up
FSEP questionnaire results	Cycle 1, 3, 6 and follow-up
PGWBI questionnaire results	Cycle 1, 3, 6 and follow-up
Vaginal pH	Cycle 1, 3, 6 and follow-up