Actively Recruiting

Phase 2
Age: 18Years - 79Years
All Genders
NCT05825092

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

Age: 18Years - 79Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

AI-Screening

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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

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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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