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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00512408
Other study ID # 002-07
Secondary ID
Status Terminated
Phase N/A
First received August 6, 2007
Last updated October 16, 2008
Start date July 2006
Est. completion date March 2007

Study information

Verified date August 2007
Source IRCCS San Raffaele
Contact n/a
Is FDA regulated No
Health authority Italy: Ethics Committee
Study type Observational

Clinical Trial Summary

Background: Patients with congestive heart failure (CHF) show muscle mass wasting and decreased testosterone levels. Long-term testosterone supplementation improves walking distance and glucose metabolism of patients CHF. No studies have investigated the integrated effects of testosterone on exercise oxygen uptake muscle strength and glucose metabolism in patients with CHF regardless of the presence of hypogonadism.

Aim: To assess the effect of a 12 week testosterone administration on maximal exercise capacity, muscle strength and insulin resistance in elderly CHF patients.

Methods: Seventy elderly patients with stable CHF, mean age 71 ± 8 years, ejection fraction 34 ± 1%, NYHA class II/III 38/32, were enrolled. Of these, 35 were randomized to receive testosterone therapy (through intramuscular injection every 6 week) and 35 to receive placebo both on top of maximal medical therapy. At baseline and after 12 weeks all patients underwent echocardiogram, cardiopulmonary test, 6-minute walking test (6MWT), quadriceps maximal isometric and isokinetic strength.


Recruitment information / eligibility

Status Terminated
Enrollment 0
Est. completion date March 2007
Est. primary completion date
Accepts healthy volunteers
Gender Male
Age group 56 Years to 76 Years
Eligibility Inclusion Criteria:

- left ventricular ejection fraction (LVEF) < 40%;

- New York Heart Association (NYHA) class II or III;

- clinical stability without hospital admission for heart failure in the previous 3 months.

Exclusion Criteria:

- unstable angina or recent acute myocardial infarction,

- history of severe liver diseases

- history of severe kidney diseases

- uncontrolled hypertension

- erythrocytosis (hematocrit > 50%)

- hyperviscosity

- prostate cancer, prostate-specific antigen (PSA) greater than 3 ng/ml

- severe lower urinary tract symptoms.

Study Design

Time Perspective: Prospective


Intervention

Drug:
testosterone


Locations

Country Name City State
Italy IRCCS San Raffaele Rome

Sponsors (1)

Lead Sponsor Collaborator
IRCCS San Raffaele

Country where clinical trial is conducted

Italy, 

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