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Anabolic Steroids for Nutritional Rehabilitation of Critically Ill Patients
This study is currently recruiting participants.
Study NCT00242463   Information provided by Lawson Health Research Institute
First Received: October 19, 2005   Last Updated: October 25, 2005   History of Changes

October 19, 2005
October 25, 2005
October 2005
 
Nitrogen Balance
Same as current
Complete list of historical versions of study NCT00242463 on ClinicalTrials.gov Archive Site
  • Lean body mass
  • serum prealbumin
  • length of stay on ventilator, in ICU, in HOSPITAL
  • infectious complications
  • outcome (mortality)
Same as current
 
Anabolic Steroids for Nutritional Rehabilitation of Critically Ill Patients
The Efficacy of Anabolic Steroids for the Nutritional Rehabilitation of Critically Ill Patients

This prospective, double-blinded study will determine the feasibility of determining the efficacy of a weekly intramuscular injection of nandrolone (an anabolic steroid) in malnourished ICU patients.The data from this study will also enable us to prepare a future grant proposal with a calculated sample size necessary to deomonstrate an improvement in clinical outcome.

Critically ill patients are particularly prone to excessive catabolism using skeletal muscle as the primary substrate as a result of maladaptation to critical illness. Ultimately, critical illness leads to a significant loss of lean body mass (LBM). For example, a 40% loss of LBM is associated with a 100% mortality. Anabolic steroids have been studied and have been shown to improve nutrition in select malnourished patient groups, however, the majority of these studies were not well designed or consisted of small sample sizes.

Our hypothesis is anabolic steroid administration will result in an augmentation of positive nitrogen balance and LBM. This increase in LBM will result in liberation from mechanical ventilation sooner than the placebo group and will result in discharge from the ICU sooner, and as a result, a reduction in morbidity (nosocomial infections) and possibly mortality.

All moderately to severly malnourished ICU patients who have an anticipated stay in ICU > 10 days, will be randomized to receive nandrolone (25 mg-females, 50 mg;males) once weekly for six weeks or placebo. All patients will receive a standard enteral nutritional regimen. Patients will be monitored for assessment of nitrogen balance, lean body mass, and length of time spent on ventilator, in ICU and in HOSP, and incidence of infections.Lean body mass will be measured using a bioimpedance analyzer.

Phase II
Interventional
Allocation:  Randomized
Control:  Placebo Control
Endpoint Classification:  Safety/Efficacy Study
Intervention Model:  Single Group Assignment
Masking:  Double-Blind
Primary Purpose:  Treatment
  • Malnutrition
  • Critical Illness
Drug: Nandrolone (anabolic steroid)
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Recruiting
20
 
 

Inclusion Criteria:

  1. anticipated length of stay in ICU >10 days
  2. moderate to severe malnutrition
  3. patient tolerating enteral feeds

Exclusion Criteria:

  1. age < 18 yrs
  2. known allergy to nandrolone
  3. women of child bearing age with positive pregancy test
  4. contraindications to intramuscular injections ie anticoagulation
  5. renal failure requiring renal replacement therapy
  6. patients with breast or prostate cancer -
Both
18 Years and older
Yes
Contact: Michael D Sharpe, MD FRCPC 519-663-3030 michael.sharpe@lhsc.on.ca
Canada
 
NCT00242463
 
R-05-390
Lawson Health Research Institute
 
Principal Investigator: Michael D Sharpe, MD FRCPC London Health Sciences Centre-UC
Lawson Health Research Institute
October 2005

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP