Fact CheckerSign in

NCT04921306CompletedPhase 2

Obese Human Beta-2-adrenergic Stimulation and Muscle Glucose Uptake

Targeting the Beta-2-adrenergic Pathway to Improve Skeletal Muscle Glucose Uptake in Obese Humans

Source: ClinicalTrials.gov · Last updated 7 May 2024

Brief summary (registry, in English)

The purpose of this study is to investigate the effect of four weeks clenbuterol/placebo supplementation on skeletal muscle glucose disposal in overweight/obese male and (postmenopausal) female volunteers.

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
14 (actual)
First submitted
25 May 2021
Start date
16 Aug 2022
Primary completion date
1 Mar 2024
Lead sponsor
Maastricht University
NCT number
NCT04921306

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 14
  • From 16 Aug 2022 to the primary completion date, 1 Mar 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Excessive alcohol and/or drug abuse;
  • Participation in another biomedical study within 1 month before the first study visit, possibly interfering with the study results;
  • Medication use known to hamper subject's safety during the study procedures;

Other illness

  • Cardiovascular disease (determined by means of questionnaires, heart rate/blood pressure measurements and an ECG)
  • Respiratory diseases (including asthma, bronchitis and COPD);
  • Epilepsy;
  • Renal and/or liver insufficiency;
  • Diagnosed with type 1 or type 2 diabetes mellitus;
  • Any contra-indications to MRI scanning. These contra-indications include patients with:
    • Electronic implants such as pacemakers, defibrillators or neurostimulators
    • Central nervous system aneurysm clip
    • Some hearing aids (such as cochlear implant) and artificial (heart) valves which are contraindicated for MRI/MRS
    • Iron containing corpora aliena in the eye or brains
    • Claustrophobia

Lab values

  • Any condition, disease or abnormal laboratory test result that, in the opinion of the Investigator, would interfere with the study outcome, affect trial participation or put the subject at undue risk;

Other

  • Not meeting all inclusion criteria
  • Unstable body weight (weight gain or loss \> 3 kg in the last three months);
  • Intention to lose or gain body weight (e.g. with caloric restriction or physical activity)
  • Hypokalaemia;
  • Hyperthyroidism
  • Anaemia;
  • Smoking;
  • Subjects who do not want to be informed about unexpected medical findings;
  • Subjects who do not want that their treating physician to be informed;
  • Inability to participate and/or complete the required measurements;
  • Participation in organised or structured physical exercise (\>2h per week);

Who the study is looking for

  • Caucasian;
  • Male or (postmenopausal; defined as 1 year after the last cycle) female;
  • Age between 40-70 years;
  • BMI: 27-35 kg/m2;

Age in the registry: 40 years to 70 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Maastricht University
Coordinator of this site? Confirm its status
MaastrichtNetherlandsUnknown status

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.