Actively Recruiting
Effects of Early Testosterone Gel Administration on Physical Performance in the Critically Ill
Led by University Hospital, Clermont-Ferrand · Updated on 2023-10-02
600
Participants Needed
5
Research Sites
192 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Critically ill patients experience major insults that lead to increased protein catabolism. Hypermetabolism occurs early and rapidly during the first week of critical illness to provide amino acids for the production of energy via gluconeogenesis, and also for the synthesis of acute phase proteins and repair of tissue damage. During acute phase, neuroendocrine and inflammatory responses promote protein breakdown and amino acid release. Under stress conditions, protein synthesis cannot match the increased rate of muscle proteolysis because of a state of anabolism resistance, which limits uptake of amino acids into muscles. Hypermetabolism results in a significant loss of lean body mass with an impact on weaning from the ventilator and muscle recovery. Functional disability can be long term sometimes with no full return to normal. In critically ill patients, severe and persistent testosterone deficiency is very common and is observed early after Intensive Care Unit (ICU) admission. This acquired hypogonadism promotes the persistent loss of skeletal muscle protein and is related to poor outcome. Administration of testosterone induces skeletal muscle fiber hypertrophy and decreases protein breakdown in healthy young men. It has been repeatedly shown that testosterone treatment enhances muscle mass and strength in hypogonadal men and women and can improve physical performance. Testosterone administration in burned patients reduces protein breakdown and increases protein synthesis efficiency. Oxandrolone, a synthetic testosterone analogue, reduces body mass and nitrogen loss and accelerates healing in burned patients. Trials in critically ill unburned patients failed to demonstrate any effect on clinical outcome but the studies were underpowered to detect a difference. Transdermal gel testosterone is the preferred route of administration for achieving steady serum testosterone concentrations as compared to oral and intramuscular formulations. Intramuscular injection induces strong fluctuations of testosterone plasma concentrations and can cause haematoma in patients with coagulation disorders, a common condition in ICUs. Several studies have raised the concern that testosterone administration could increase the risk of cardiovascular disease events. However, in a recent meta-analysis, no significant effects on cardiovascular risk were observed with either injected or transdermal testosterone supplementation in men, and the French National Agency for Medicines (ANSM) recently reported that drugs containing testosterone were not associated with an increased risk of cardiovascular events.
CONDITIONS
Official Title
Effects of Early Testosterone Gel Administration on Physical Performance in the Critically Ill
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Males and females aged over 18 years
- Negative pregnancy test (b-HCG) in female patients of childbearing potential
- Expected need for invasive mechanical ventilation for more than 48 hours
- Written informed consent from patient or legal representative
- Social security coverage
- Use of contraception by female patients of childbearing potential and their male partners during treatment and for months after
- Male patients with female partners of childbearing potential agree to effective contraception during treatment and for months after
You will not qualify if you...
- History or suspicion of prostate cancer
- History or suspicion of breast cancer
- Prostatic specific antigen (PSA) level 64 ng/ml
- ICU stay longer than 120 hours before enrollment
- Moribund condition
- Pre-existing illness with life expectancy under 6 months
- Recent intracranial or spinal cord injury under 1 month
- Recent hemorrhagic or ischemic stroke under 1 month
- Neuromuscular disease
- Cardiac arrest in non-shockable rhythm
- Pre-existing cognitive impairment or language barrier
- Inability to walk without assistance before ICU illness
- Documented allergy to testosterone
- Age over 80 years
- Pregnancy or breastfeeding
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Trial Site Locations
Total: 5 locations
1
Service de Medecine Intensive et Réanimation CHU de Bordeaux Hopital Pellegrin
Bordeaux, France
Not Yet Recruiting
2
Service d'Anesthésie et Réanimation Centre Jean-Perrin
Clermont-Ferrand, France
Actively Recruiting
3
Service de Médecine Intensive et Réanimation (MIR), CHU Clermont-Ferrand
Clermont-Ferrand, France
Actively Recruiting
4
Service de Médecine Intensive et de Réanimation CHD La Roche sur Yon
La Roche-sur-Yon, France
Actively Recruiting
5
Service de Médecine Intensive et Réanimation CHU Nantes, Hôtel Dieux
Nantes, France, 44000
Actively Recruiting
Research Team
L
Lise LACLAUTRE
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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