Skip to content

Effect of transdermal testosterone replacement in hypogonadal men with decreased insulin sensitivity

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN45741714
Enrollment
320
Registered
2006-02-06
Start date
2006-01-31
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Hypogonadal men with decreased insulin sensitivity Nutritional, Metabolic, Endocrine Testicular hypofunction

Interventions

Once daily testosterone replacement gel 2% versus placebo gel

Sponsors

ProStrakan Pharmaceuticals (UK)
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1. Hypogonadal males 2. Decreased insulin sensitivity

Exclusion criteria

Exclusion criteria: 1. Use of testosterone replacement therapy in the last six months 2. History of or current prostate carcinoma

Design outcomes

Primary

MeasureTime frame
Change in insulin sensitivity

Secondary

MeasureTime frame
1. Change in abdominal obesity, lipid profile and glycaemic control 2. Change in symptoms of hypogonadism 3. The safety and tolerability of testosterone replacement gel compared to placebo gel

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026