- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06152497
The Role of Histamine in Muscle Protein Synthesis Following Resistance Training
December 6, 2023 updated by: University Ghent
The Role of Histamine in Muscle Protein Synthesis Following Chronic Resistance Training
Blocking histamine H1/H2 receptors blunts chronic endurance training adaptations.
The current study addresses the following research question: "What is the influence of histamine H1 signaling on training adaptations following ten weeks of resistance training in human skeletal muscle."
Results from this study will yield more insights into the molecular mechanisms of adaptations to exercise training.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
50
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: Wim Derave, Professor
- Phone Number: +32 92646326
- Email: wim.derave@ugent.be
Study Locations
-
-
Oost-Vlaanderen
-
Ghent, Oost-Vlaanderen, Belgium, 9000
- Recruiting
- Department of movement and sports sciences, Ghent University, Belgium
-
Contact:
- Wim Derave, Professor
- Phone Number: +32 92646326
- Email: wim.derave@ugent.be
-
-
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
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Male
- 18-45 years
- Not to medium physically active
Exclusion Criteria:
- Smoking
- Chronic disease
- High blood pressure
- Supplement or medication intake
- Seasonal allergies
- Vegetarian / vegan
- Resistance trained
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 Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Placebo Comparator: 1: Placebo
Lactose
|
Oral placebo
Resistance training: lower body exercise
|
|
Experimental: H1 blockade: Telfast (180mg Fexofenadine)
H1: Telfast (180mg Fexofenadine)
|
Resistance training: lower body exercise
H1 blockade: oral blockade with 180mg Fexofenadine
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Muscle volume
Time Frame: Before and after the 10 weeks of resistance training
|
Change in muscle volume
|
Before and after the 10 weeks of resistance training
|
|
Maximal dynamic strength of leg press, bench press, bicep curl and leg curl
Time Frame: Before and after the 10 weeks of resistance training
|
Change in maximal dynamic strength of leg press, bench press, bicep curl and leg curl
|
Before and after the 10 weeks of resistance training
|
|
Muscle fiber hypertrophy in muscle biopsies
Time Frame: Before and after the 10 weeks of resistance training
|
Change in muscle fiber hypertrophy in muscle biopsies
|
Before and after the 10 weeks of resistance training
|
|
Vascular function measured with a single passive leg movement (sPLM: change in femoral blood flow measured with Doppler ultrasound before and after one passive flexion/extension of the leg)
Time Frame: Before and after the 10 weeks of resistance training
|
Change in vascular function with a single passive leg movement (sPLM: change in femoral blood flow measured with Doppler ultrasound before and after one passive flexion/extension of the leg)
|
Before and after the 10 weeks of resistance training
|
|
Matsuda index, to estimate whole body glucose metabolism, will be calculated using an oral glucose tolerance test (OGTT: concentration of glucose and insulin in the blood will be measured before and after drinking 75g glucose)
Time Frame: Before and after the 10 weeks of resistance training
|
Change in Matsuda index, to estimate whole body glucose metabolism, will be calculated using an oral glucose tolerance test (OGTT: concentration of glucose and insulin in the blood will be measured before and after drinking 75g glucose)
|
Before and after the 10 weeks of resistance training
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Blood pressure (systolic and diastolic)
Time Frame: Before and after the 10 weeks of resistance training
|
Chance in Blood pressure (systolic and diastolic)
|
Before and after the 10 weeks of resistance training
|
|
Resting heart rate
Time Frame: Before and after the 10 weeks of resistance training
|
Chance in Resting heart rate
|
Before and after the 10 weeks of resistance training
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Wim Derave, Professor, University Ghent
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 (Actual)
September 1, 2023
Primary Completion (Estimated)
December 31, 2026
Study Completion (Estimated)
December 31, 2026
Study Registration Dates
First Submitted
December 20, 2022
First Submitted That Met QC Criteria
November 29, 2023
First Posted (Actual)
November 30, 2023
Study Record Updates
Last Update Posted (Estimated)
December 13, 2023
Last Update Submitted That Met QC Criteria
December 6, 2023
Last Verified
December 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- MPSH - ONZ-2023-0027
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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