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The Effect of Nandrolone Decanoate and Leucine on Muscle Loss

The Effect of Nandrolone Decanoate Injection and Leucine Supplementation on Muscle Loss

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02376309
Acronym
Le-Na
Enrollment
30
Registered
2015-03-03
Start date
2015-08-31
Completion date
2017-08-31
Last updated
2017-08-29

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

Conditions

Muscle Atrophy

Brief summary

A decrease in muscle mass can have a profound impact on quality of life, as it can lead to decreased strength, insulin resistance, lower basal metabolic rate and obesity. With this study we investigate whether ingesting leucine or getting a ND injection will reduce the loss of muscle mass and strength.

Interventions

BEHAVIORALInactivity

Inactivity

DRUGND

1 nandrolone decanoate injection

DIETARY_SUPPLEMENTLeu

Leucine supplements

Sponsors

Maastricht University Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy men 18-35 years * BMI between 18.5 and 30 kg/m2

Exclusion criteria

\- (Family) history of thromboembolic events * Smoking * Recent surgery (within 6 months prior to the study) * Performing progressive resistance training more than three times per week in the past year * Any back/leg/knee/shoulder complaints which may interfere with the use of crutches * Current systemic use of corticosteroids, anabolic steroids, growth hormone, testosterone, nandrolone, protein supplements, immunosuppressants or insulin, blood sugar decreasing medication or EPO * All co-morbidities interacting with mobility and muscle metabolism of the lower limbs (e.g. arthritis, spasticity/rigidity, all neurological disorders and paralysis) * Use of anti-coagulants * Pre-existing renal disease or those with a potential risk for renal dysfunction (diabetes, hypertension, reduced glomerular filtration rate) * Liver disease * Heart failure * Migraine * Allergy to nuts or soy * High blood pressure (\>140 mmHg systolic and \>90 mmHg diastolic) In case of doubt, in- or exclusion of subject will be discussed with responsible physician or principal investigator.

Design outcomes

Primary

MeasureTime frameDescription
CSA Quadriceps (CT scan)7 daysCT scan

Secondary

MeasureTime frame
Muscle strength as measured by 1RM test7 days
Muscle fiber type and CSA as measured by histochemistry from the muscle biopsy7 days

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026