- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02557581
cAMP Signaling and Muscle Adaptations
October 25, 2017 updated by: Morten Nielsen, University of Copenhagen
The role of cAMP signaling mediated by beta2-adrenergic stimulation with agonists has been well-studied in skeletal muscles of animals.
Studies in humans are scant and the scope of the present study is thus to investigate the role of cAMP signaling by beta2-adrenergic stimulation for muscle adaptations in humans.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Anticipated)
72
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Morten Hostrup, PhD
- Phone Number: +4524474785
- Email: mortenhostrup@gmail.com
Study Locations
-
-
-
Copenhagen, Denmark, 2100
- Recruiting
- Department of Nutrition, Exercise and Sports
-
Contact:
- Morten Hostrup, PhD
- Phone Number: +4524474785
- Email: mortenhostrup@gmail.com
-
Copenhagen, Denmark, 2400
- Recruiting
- Bispebjerg University Hospital
-
Contact:
- Morten Hostrup, PhD
- Phone Number: +4524474785
- Email: mortenhostrup@gmail.com
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 35 years (ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Male
Description
Inclusion Criteria:
- healthy young men
- 18-35 years of age
- Informed consent
- Active 2-5 hours of training pr. week
- Maximal oxygen uptake (ml/min/kg) of 40-60
- Lean body mass of 55-65 kg / Lean mass index 14-22 kg/m2
Exclusion Criteria:
- Smoker
- Allergy towards study drugs
- Chronic disease
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: BASIC_SCIENCE
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: TRIPLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
PLACEBO_COMPARATOR: Placebo
|
|
EXPERIMENTAL: Terbutaline
Beta2-adrenergic stimulation with terbutaline
|
|
EXPERIMENTAL: Clenbuterol
Beta2-adrenergic stimulation with clenbuterol
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Muscle hypertrophy (lean body mass in Kilograms)
Time Frame: 2 days
|
Lean body mass (kg) will be measured at two different days by Dual X-ray absorbance (DXA)
|
2 days
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Energy turnover (ml/min or mmol/kg dry weight muscle)
Time Frame: 1 day
|
Pulmonary gas exchange and lactate and glycogen will be measured in muscle biopsies obtained before and after intense exercise
|
1 day
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
July 1, 2015
Primary Completion (ACTUAL)
June 30, 2017
Study Completion (ANTICIPATED)
October 1, 2017
Study Registration Dates
First Submitted
September 13, 2015
First Submitted That Met QC Criteria
September 22, 2015
First Posted (ESTIMATE)
September 23, 2015
Study Record Updates
Last Update Posted (ACTUAL)
October 26, 2017
Last Update Submitted That Met QC Criteria
October 25, 2017
Last Verified
October 1, 2017
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Pathological Conditions, Anatomical
- Hypertrophy
- Physiological Effects of Drugs
- Adrenergic Agents
- Neurotransmitter Agents
- Molecular Mechanisms of Pharmacological Action
- Autonomic Agents
- Peripheral Nervous System Agents
- Adrenergic Agonists
- Bronchodilator Agents
- Anti-Asthmatic Agents
- Respiratory System Agents
- Reproductive Control Agents
- Adrenergic beta-2 Receptor Agonists
- Adrenergic beta-Agonists
- Tocolytic Agents
- Sympathomimetics
- Terbutaline
- Clenbuterol
Other Study ID Numbers
- TUD
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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