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Testosterone Replacement in Diabetes With Vascular Disease (Version 2)

A Randomised, Double Blind, Placebo-controlled Parallel Study to Test the Effect of Testosterone Treatment on Peripheral Vascular Disease in Hypogonadal Men With Type 2 Diabetes Mellitus

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00355537
Enrollment
19
Registered
2006-07-24
Start date
2006-02-28
Completion date
2009-12-31
Last updated
2010-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetes Mellitus, Peripheral Vascular Disease

Brief summary

Diabetes is a major cause of peripheral vascular disease(PVD) and is associated with male hypogonadism. Diabetes and PVD are both associated with arterial stiffness and intima -media thickness which are also related to severity of the clinical syndrome of PVD. Artificially induced hypogonadism results in increasing arterial stiffness whilst testosterone is known to improve risk factors for vascular disease and act as a vasodilator. The purpose of this pilot study is to assess the effect of testosterone treatment on PVD arterial stiffness and intima-media thickness in men with type 2 diabetes and hypogonadism,

Interventions

DRUGTestosterone

Sustanon- intramuscular testosterone 200mg every 2 weeks

DRUG0.9% saline

Saline injection intramuscular every 2 weeks

Sponsors

Barnsley Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Male patients greater than 18 years of age * Type 2 Diabetes Mellitus * Serum testosterone less than 11 nmol/L on two consecutive samples taken on different days * Peripheral vascular disease as defined by ABPI less than 0.92 and ischaemic leg pain (claudication or rest pain) or distal complications (non-healing arterial foot ulcer or gangrene * Agreement to maintain antihypertensive and anti-lipid treatments at prior doses during 3 months of study * Ability to give written informed consent after verbal and written explanation in the English Language * Ability to comply with all study requirements

Exclusion criteria

* Current or previous breast cancer * Current or previous prostate cancer * Raised prostate specific antigen or abnormal per rectal examination unless prostate cancer excluded after specialist urology opinion * Severe symptoms of benign prostatic hypertrophy ('prostatism') * Treatment with testosterone in the 3 months prior to the trial * Investigational drug treatment in the 3 months prior to the trial

Design outcomes

Primary

MeasureTime frame
The effect of testosterone replacement on arterial stiffness measured by ultrasound derived index B of the femoral artery in men with a combination of DM, PVD and hypogonadism.3 months

Secondary

MeasureTime frame
The effect of testosterone on intima-media thickness of the femoral artery measured by ultrasound .3 months
The effect of testosterone on peripheral circulation in legs affected by PVD as measured by transcutaneous oxygen saturation in the feet of the study population.3 months
The effect of testosterone on PVD as measured by ankle-brachial-pressure-indices (ABPI) .3 months
The effect of testosterone on markers of vascular risk; blood pressure, serum-lipid levels, weight, waist circumference, body fat percentage, urinary micro-albumin concentration and C reactive protein levels.3 months

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026