Reandron in Diabetic Men Witn Low Testosterone Level
Primary Purpose
Type 2 Diabetes, Hypogonadism
Status
Completed
Phase
Phase 2
Locations
Australia
Study Type
Interventional
Intervention
Reandron 1000
placebo
Sponsored by
About this trial
This is an interventional treatment trial for Type 2 Diabetes
Eligibility Criteria
Inclusion Criteria:
- Type 2 diabetes
- Testosterone less than 10 nmol/L
Exclusion Criteria:
- Contraindication to
- Testosterone or
- IM injection
Sites / Locations
- Austin Health
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
1
2
Arm Description
Reandron 100 treatment
Placebo
Outcomes
Primary Outcome Measures
Insulin Resistance
Secondary Outcome Measures
Bone microarchitecture
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00613782
Brief Title
Reandron in Diabetic Men Witn Low Testosterone Level
Official Title
Testosterone Replacement Therapy in Men With Type 2 Diabetes Mellitus and Low Testosterone Levels
Study Type
Interventional
2. Study Status
Record Verification Date
June 2012
Overall Recruitment Status
Completed
Study Start Date
January 2009 (undefined)
Primary Completion Date
January 2014 (Actual)
Study Completion Date
April 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Austin Health
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
In men with type 2 diabetes, low testosterone levels have been associated with insulin resistance, truncal obesity and symptoms such as fatigue and erectile dysfunction. Low testosterone may impair cardiac function and increase cardiovascular risk and cause osteoporosis. The goal of this project is to assess prospectively whether, in men with type 2 diabetes mellitus and low testosterone levels, testosterone replacement improves insulin resistance, body composition, bone density, cardiac function symptoms associated with low testosterone level.
The investigators will recruit 140 ambulatory men with type 2 diabetes and a low serum testosterone level (<10 nmol/L) from Austin Health Endocrine clinics, General Practise surgeries, and from the general public by direct consumer advertising via newspaper and other local media. Men will be randomised to either intramuscular testosterone undecanoate (Reandron 1000, Bayer Schering Pharma) or placebo. Men with contraindications to testosterone replacement or to intramuscular injections will be excluded from the study. All men will receive intramuscular testosterone or placebo injections at 0, 6, 18 and 30 weeks (a total of four injections).
All 140 study subjects will have a clinical and laboratory assessment at baseline, 18 weeks and at study end (40 weeks). All 140 subjects will also have imaging studies at baseline and at study end (40 weeks). The study protocol is outlined in more detail below:
Clinical and laboratory assessment (Baseline and repeated 18 weeks, 40 weeks) A full medical history and physical examination will be performed. Symptoms will be assessed by the following standardised questionnaires: 1) Androgen Deficiency in the Aging Male (ADAM); 2) Aging Male Symptom scale (AMS); 3) International Index of Erectile Dysfunction (IIED); 4) International Prostate Symptom Score (IPSS); 5) SF-36 (all five questionnaires are attached to Module 1).
Laboratory studies will consist of blood tests to measure total testosterone, fasting glucose, C-peptide, HBA1c and other routine parameters.
Imaging studies (Baseline and repeated at 40 weeks)
Body composition and bone mineral density by DEXA
Body composition by magnetic resonance imaging
Bony micro-architecture by high resolution quantitative computed tomography [HR-pQCT]),
Cardiac dimensions and function by transthoracic doppler echocardiography
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 2 Diabetes, Hypogonadism
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Single Group Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
88 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Active Comparator
Arm Description
Reandron 100 treatment
Arm Title
2
Arm Type
Placebo Comparator
Arm Description
Placebo
Intervention Type
Drug
Intervention Name(s)
Reandron 1000
Other Intervention Name(s)
testosterone undecanoate
Intervention Description
1000mg at 0,6,18,30 weeks
Intervention Type
Drug
Intervention Name(s)
placebo
Intervention Description
placebo injection 0,6.18.30 weeks
Primary Outcome Measure Information:
Title
Insulin Resistance
Time Frame
40 weeks
Secondary Outcome Measure Information:
Title
Bone microarchitecture
Time Frame
40 weeks
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Type 2 diabetes
Testosterone less than 10 nmol/L
Exclusion Criteria:
Contraindication to
Testosterone or
IM injection
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mathis Grossmann
Organizational Affiliation
Austin Health
Official's Role
Principal Investigator
Facility Information:
Facility Name
Austin Health
City
Melbourne
State/Province
Victoria
ZIP/Postal Code
3084
Country
Australia
12. IPD Sharing Statement
Citations:
PubMed Identifier
24978674
Citation
Gianatti EJ, Dupuis P, Hoermann R, Zajac JD, Grossmann M. Effect of testosterone treatment on constitutional and sexual symptoms in men with type 2 diabetes in a randomized, placebo-controlled clinical trial. J Clin Endocrinol Metab. 2014 Oct;99(10):3821-8. doi: 10.1210/jc.2014-1872. Epub 2014 Jun 30.
Results Reference
derived
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Reandron in Diabetic Men Witn Low Testosterone Level
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