Oral Testosterone for Fatigue in Male Multiple Sclerosis Patients

Multiple Sclerosis Clinical Trial

Official title:

A Randomized, Controlled Crossover Trial Evaluating Oral Testosterone in the Treatment of Fatigue in Male Multiple Sclerosis Patients

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT01516554
• Other study ID #: 38486
• Secondary ID: 812.14
• Status: Terminated
• Phase: Phase 2
• First received: January 19, 2012
• Last updated: July 4, 2014
• Start date: February 2012
• Est. completion date: July 2014

Study information

• Verified date: July 2014
• Source: Health Sciences Centre, Winnipeg, Manitoba
• Contact: n/a
• Is FDA regulated: No
• Health authority: Canada: Health Canada
• Study type: Interventional

Clinical Trial Summary

Fatigue is one of the most frequent symptoms reported by multiple sclerosis (MS) patients and is often a significant source of disability. Unlike normal fatigue, multiple sclerosis related fatigue (MSRF) occurs independently of activity level, suggesting that it is due to dysfunction in the neural pathways that regulate the perception of energy although the precise cause is still not understood. While MSRF can be managed through lifestyle modifications and with drug treatment, these measures are commonly either ineffective or only partially effective.

Administration of the male sex hormone testosterone has been shown to improve energy levels in males with testosterone-deficiency states. Testosterone also reduces fatigue in patients with other medical conditions not associated with low testosterone levels, suggesting that this treatment may also be useful in symptomatic control of MSRF.

This proposed seven-month long clinical trial is designed to test the hypothesis that administration of oral testosterone tablets to male MS patients will result in an improvement of fatigue relative to the administration of placebo tablets. As fatigue is frequently reported by MS patients to be one of their most frustrating and disabling symptoms, any proven additional treatment option for MSRF would be beneficial in improving quality of life.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 3
• Est. completion date: July 2014
• Est. primary completion date: January 2014
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• All adult male (18—65 years old) patients are eligible. Patients over > 65 years will be excluded due to increased risk of prostatic hypertrophy or carcinoma in that age group.

• Patients must have diagnosis of MS using the 2005 revised McDonald Criteria.

• Patients must have an EDSS score = 6.5.

• Patients must have a baseline MFIS score = 45 (i.e.: those patients with fatigue).

• Patients must consent to participate in the study after a discussion of the potential risks and benefits of study participation with their physician. This consent must acknowledge that testosterone administration in MS is experimental and of no proven benefit.

• Patients must not be on any other agents to specifically treat MSRF (modafinil [Alertec®], amantadine, methylphenidate [Ritalin®, Ritalin SR®, Concerta®].

Exclusion Criteria:

• Previous or current testosterone administration.

• Any Health Canada approved indication for testosterone administration.

• Known hypersensitivity any component of the testosterone undecanoate (Andriol®) formulation including soy.

• History of relapse in the past 3 months.

• History of prostate hypertrophy or prostate carcinoma.

• History of breast cancer.

• Moderate or severe prostate symptoms (International Prostate Symptom Score [IPSS] = 8).

• All patients = 50 years old (or = 40 years old if history of prostate cancer/prostate hypertrophy in a first-degree relative or if African-Canadian) will be require a urological assessment including prostate specific antigen (PSA) and digital rectal exam (DRE). Such patients will be excluded if they have a high PSA level or if they have a palpable prostate nodule. Abnormal PSA levels will be determined using standard age-specific cut-off levels.

• Other serious medical comorbidities including: any other cancer or myelodysplastic syndrome, anemia or polycythemia of any cause, vascular risk factors (including hypertension, dyslipidemia, myocardial infarction, stroke, peripheral vascular disease, atrial fibrillation, other hypercoaguable state or thrombotic risk factor), serious kidney or liver disease, diabetes, obstructive sleep apnea or serious psychiatric disease.

• History of current alcohol misuse.

• Recent major surgery.

• Use of the following medications whose metabolism may be altered by TT: warfarin, corticosteroids, propranolol, cyclosporine or St. John's Wort.81

• Patients on cyclophosphamide or mitoxantrone (Novantrone®) chemotherapy for MS will be excluded. Patients on other approved disease-modifying therapies for MS (interferon-ß1a [Avonex®, Rebif®], interferon-ß1b [Betaseron®], glatiramer acetate [Copaxone®] and natalizumab [Tysabri®]) can participate in this trial provided they have been on these therapies for at least six months at a stable dose.

Study Design

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

Related Conditions & MeSH terms

• Fatigue
• Multiple Sclerosis
• Sclerosis

Intervention

Drug:
• Testosterone undecanoate
40 mg twice daily
• placebo
twice daily

Locations

Country	Name	City	State
Canada	Health Sciences Centre	Winnipeg	Manitoba

Sponsors (4)

Lead Sponsor	Collaborator
Health Sciences Centre, Winnipeg, Manitoba	Consortium of Multiple Sclerosis Centers, Manitoba Medical Service Foundation, University of Manitoba

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in fatigue (measured with Modified Fatigue Impact Scale [M-FIS])		baseline and 12 weeks	No
Secondary	Change in fatigue as measured on a visual analog scale (VAS)		baseline and 12 weeks	No
Secondary	Quality of life as measured with the Aging Males' Symptoms (AMS) scale		baseline and 12 weeks	No
Secondary	Neurological status as measured with the Expanded Disability Status Scale (EDSS)		baseline and 12 weeks	No
Secondary	Number of participants with , type and severity of adverse events		12 weeks	Yes