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Beta2-adrenergic Agonism and Muscle Remodelling

M

Morten Hostrup, PhD

Status

Unknown

Conditions

Physiologic Hypertrophy
Physical Activity
Hypertrophy

Treatments

Drug: Formoterol
Other: Placebo
Drug: Terbutaline

Study type

Interventional

Funder types

Other

Identifiers

NCT03565302
FOR/TER

Details and patient eligibility

About

The study aims to investigate gender-specific adaptations to beta2-adrenoceptor stimulation with selective short- and long-acting beta2-agonist with emphasis on skeletal muscle in relation to performance enhancing effects and anti-doping

Enrollment

72 estimated patients

Sex

All

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy men and women, aged 18-45 years
  • VO2max >55 ml/kg/min for men and >50 ml/kg/min for women (± biologic and techinical variation of 5.6% (Katch et al. 1982)
  • Body Mass Index (BMI) < 26

Exclusion criteria

  • Chronic user of beta2-agonist or allergy towards study drugs
  • Serious adverse side effects of the used study drug
  • Chronic disease that by the project physician would affect any of the outcomes of the study
  • Smoker
  • Chronic use of prescription medication (other than contraceptives for women)
  • Pregnancy

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

72 participants in 3 patient groups, including a placebo group

Control
Placebo Comparator group
Description:
Subjects receive placebo treatment
Treatment:
Other: Placebo
Long acting beta2-agonist
Experimental group
Description:
Subjects are treated with long-acting beta2-agonist formoterol
Treatment:
Drug: Formoterol
Short acting beta2-agonist
Experimental group
Description:
Subjects are treated with short-acting beta2-agonist terbutaline
Treatment:
Drug: Terbutaline

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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