Older Men and Testosterone

September 2, 2011 updated by: University Hospital of North Norway

Male hypogonadism is a clinical situation characterized by a low serum testosterone level in combination with a diversity of symptoms and signs such as reduced libido and vitality, decreased muscle mass, increased fat mass and depression. Similar symptoms in combination with subnormal testosterone levels are seen in some elderly men. Low testosterone levels are associated with known cardiovascular risk factors, and men with diabetes and stroke have lower testosterone levels than healthy men. Even though several publications have suggested that testosterone treatment in hypogonadal men may have beneficial effects, it is still uncertain if testosterone substitution in the aging man is indicated. Despite this uncertainty the sale of testosterone has increased enormously the last few years.

We hypothesize that older men with subnormal testosterone levels have a varying degree of dysfunction/symptoms both physically and mentally, and that these dysfunction/symptoms can be improved with testosterone treatment.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Older men and testosterone (Short version of the study protocol)

Cohort study "How is life as an elderly man when serum testosterone is subnormal?"

To investigate whether subnormal testosterone levels in elderly men (60-80 years old) is associated with clinical symptoms and/or disease, the investigators will ask men with normal testosterone (>11.3 nmol/l) and men with subnormal testosterone levels (<11.3 nmol/l) who participated in the last Tromsø study 2001 to participate in this study.

Screening: Blood pressure, clinical examination including prostate examination, blood samples (testosterone, SHBG, LH, FSH, albumin and PSA).

Aproximately 350 men had subnormal testosterone levels in the last Tromsø study and the researchers will try to include up to 200 men who still have subnormal testosterone levels and up to 200 age matched men who still have normal testosterone levels.

Procedures

Symptoms: Aging Male Symptom Score

Muscle strength and function: The researchers will investigate muscle strength, peak torque with isokinetic dynamometry in the knee joint and muscle function (gait, balance and movement); Grip Strength

Neuropsychological tests

  • Cognitive function level: WAIS
  • Memory: Wechslers Memory Scale Revised (WMS-R)
  • Trail making A and B.
  • Attention and concentration: Knox cube
  • Cognitive flexibility: Word fluency test and Stroop test
  • Quality of life: GHQ - 30 with Likert score
  • Depression: Beck Depression Inventory

The metabolic syndrome

  • DEXA (Lunar Prodigy): *Whole body, body composition; *Lumbar spine and hip, bone mineral density
  • CT scan of the abdomen to distinguish intra vs. subcutaneous fat deposits.
  • Oral glucose tolerance test.
  • Lipid profile /per oral fat load. (80 men will take part in this investigation)
  • Examination of the androgen receptor, especially the CAG and GGN polymorphism of the androgen receptor has been associated with glucose and fat metabolism.
  • Blood pressure and heart rate.
  • Neuroendocrine regulation: LH, FSH, SHBG, estradiol, testosterone, cortisol, ACTH, IGF-1, IGFBP-3, TSH, FT4, prolactin and leptin.
  • Sleep

Interventions study "Should subnormal testosterone levels be treated?"

To investigate whether older men with subnormal testosterone levels would benefit from physiological testosterone supplementation, the men with subnormal testosterone levels participating in the cohort study (approximately 150-200 men) will be asked to participate in a one year intervention study.

Randomization and treatment:

Double blind randomized (1:1) 1-year study. First injection at inclusion, second after 6 weeks, the third injection after 16 weeks, the fourth at 28 weeks and the last at 40 weeks. Active treatment is Nebido, 1000 mg testosteron undecanoate, a 4 ml intramuscular depot injection. Schering AS will supply the study with both Nebido and placebo (containing "castor oil" and "benzyl benzoate").

Registration of adverse events:

All adverse events will be recorded in the participants CRF. Serious adverse events will be reported according to regulations.

Procedures:

The above-described procedures for the cohort study will also be performed in the intervention study.

Testosterone levels, hematocrit, creatinine, ALAT and PSA will be controlled at every visit.

Object variables for both the cohort and intervention study

Primary:

Psychosexual quality of life; Muscle strength

Secondary:

Muscle function; Body composition; Intraabdominal vs. subcutaneous fat distribution; CAG and GGN polymorphism in the androgen receptor gene; Bone mineral density; Per oral glucose tolerance test; Lipid profile/fat tolerance test; Neuropsychological test; Neuroendocrine regulation Sleep

Statistics and methods:

The study will be performed at the Clinical research ward at the University Hospital of North Norway.

Comparisons between the groups will be assessed with non-parametrical tests (Mann-Whitney U-test) or ANOVA with a significant level p<0.05. In the intervention study delta-values will be used to assess changes during treatment and differences between the study groups. SPSS will be used as statistical program.

Inclusion of patients to the cohort study should be completed during 2006 and the intervention study should be completed during 2007.

Research partner Johan Svartberg, Department of Medicine, University Hospital of North Norway, Tromsø, Norway is the responsible investigator.

Partners: Professor Rolf Jorde and John-Bjarne Hansen MD, PhD, Department of Medicine, Professor Johan Sundsfjord, Department of Clinical Chemistry and Professor Knut Waterloo, Department of Neurology, University Hospital of North Norway, Tromsø, Norway and Professor Aleksander Giwercman, Scanian Andrology Center, Department of Urology, Malmö University Hospital, Sweden.

Study Type

Interventional

Enrollment

200

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Norway
      • Tromsø, Norway, 9038
        • Department of Medicine, University Hospital of North Norway

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

58 years to 78 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Male

Description

Inclusion Criteria:

  • Men 60-80 years old
  • Serum-testosterone levels <11.0 nmol/l
  • Signed informed consent.

Exclusion Criteria:

  • Prostate cancer
  • Breast cancer
  • Liver tumor/cancer
  • Unstable angina
  • Untreated congestive heart disease
  • Epilepsy
  • Migraine
  • Hematocrit >50%
  • PSA >4.0 ug/l
  • Serum creatinine >130 umol/l
  • ALAT >100 U/l
  • Known intolerance to testosterone undecanoate
  • Participation in another research trial.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Quality of life (psycho-sexual)
Muscle strength

Secondary Outcome Measures

Outcome Measure
Body composition
Muscle function
Intra abdominal vs subcutanous fat mass.
Bone density
CAG and GGN polymorphy in the androgene receptor gene
Glucose tolerance/insulin resistance
Fat tolerance
Neuroendocrine profile
Neuropsychological profile
Sleep

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

University Hospital of North Norway

Investigators

  • Principal Investigator: Johan Svartberg, MD, PhD, University Hospital of North Norway

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

September 1, 2005

Study Completion (Actual)

December 1, 2007

Study Registration Dates

First Submitted

July 5, 2005

First Submitted That Met QC Criteria

July 5, 2005

First Posted (Estimate)

July 13, 2005

Study Record Updates

Last Update Posted (Estimate)

September 5, 2011

Last Update Submitted That Met QC Criteria

September 2, 2011

Last Verified

September 1, 2011

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • Eldre menn og testosteron

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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