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Muscle Memory After Treatment With Anabolic Substance Clenbuterol and Resistance Training in Humans

Muscle Memory After Treatment With Anabolic Substance Clenbuterol and Resistance Training in Humans: Myonuclear Addition, Hypertrophy and Myocellular Reprogramming

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05692856
Enrollment
60
Registered
2023-01-20
Start date
2023-02-01
Completion date
2025-08-01
Last updated
2023-01-20

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

Conditions

Skeletal Muscle Physiology

Brief summary

The purpose of the project is investigate muscle memory and underlying mechanisms in humans following resistance training and use of the anabolic substance clenbuterol.

Interventions

Participants ingest 80 micrograms clenbuterol daily during the initial 8-week period. This period is followed by a washout of 16 weeks with no drug and resistance training. Thereafter, an 8-week period with supervised resistance training is commenced, with no drug.

DRUGPlacebo

Participants ingest placebo tablets daily during the initial 8-week period. This period is followed by a washout of 16 weeks with no drug and resistance training. Thereafter, an 8-week period with supervised resistance training is commenced, with no drug.

Sponsors

Morten Hostrup, PhD
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy men and women * BMI of \<26 and normal ECG and blood pressure

Exclusion criteria

* Smoking * Chronic disease, * Use of prescription medication * Pain due to current or previous musculoskeletal injury * Resistance training more than once per week in the 12 months leading up to the intervention * Current or previous use of prohibited anabolic substances

Design outcomes

Primary

MeasureTime frameDescription
Fiber cross-sectional areaThe change in fiber cross-sectional is assessed at baseline, 8, 24 and 32 weeksImmunohistochemistry to determine fiber cross-sectional area
MyonucleiThe change in myonuclei is assessed at baseline, 8, 24 and 32 weeksImmunohistochemistry to determine number of myonuclei
Skeletal muscle proteomeThe change in the muscle proteome is assessed at baseline, 8, 24 and 32 weeksPathway enrichment analysis of the muscle proteome using mass-spectrometry based proteomics

Secondary

MeasureTime frameDescription
Sprint performanceThe change in sprint performance is assessed at baseline, 8, 24 and 32 weeksWork performed (W) during a sprint on a bicycle ergometer
Lean massThe change in lean mass is assessed at baseline, 8, 24 and 32 weeksLean mass assessed by dual X-ray absorptiometry (DXA)
Satellite cellsThe change in satellite cells is assessed at baseline, 8, 24 and 32 weeksImmunohistochemistry to determine number of satellite cells
Isometric muscle strengthThe change in maximal voluntary isometric contraction is assessed at baseline, 8, 24 and 32 weeksMaximal voluntary isometric contraction of m. quadriceps
Dynamic muscle strengthThe change in 1-repetition maximum is assessed at baseline, 8, 24 and 32 weeks1-repetition maximum

Countries

Denmark

Contacts

Primary ContactMorten Hostrup
mhostrup@nexs.ku.dk+4535321595

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 14, 2026