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CarnosineNCT05723939

Carnosine Supplementation and Cardiovascular Function

A study testing Carnosine supplementation in people with Carnosine, run by Josip Juraj Strossmayer University of Osijek at 1 site in Croatia.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Carnosine is a dipeptide synthesized in the body from β-alanine and L-histidine. It was originally discovered in skeletal muscle where it is present in larger amounts than in other tissues, but it is also found in high concentrations in the brain, heart, and gastrointestinal tissues of humans. Read more about this study

Who is it for?
Ages 18 to 39 yearsHealthy volunteers can take part
Conditions the study is for
Carnosine
What is being tested?
Carnosine supplementation
Type of treatment
Pill or oral medicine
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
100 participants
Where
1 siteCroatia
Study dates
1 Sep 2022to 30 Jun 2024
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 39 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • young healthy sedentary individuals - did not perform regular physical activities for at least 12 months before conducting the study
  • young healthy active athletes - have a minimum of 5 training sessions per week (mainly endurance training) for at least 12 months prior to conducting the study

Who cannot join

  • smoking
  • hypertension
  • coronary disease
  • diabetes
  • hyperlipidemia
  • kidney damage
  • cerebrovascular and peripheral artery diseases
  • and any other disease that could have an impact on vascular and endothelial function

Trial locations and contacts

1 site in 1 country.

Ines Drenjančević, MD, PhD contact

+385-31-51-28-00

ines.drenjancevic@mefos.hr

Croatia1 site, 1 recruiting
  • Scientific Center of Excellence for Personalized Health Care, Josip Juraj Strossayer University of Osijek

    Osijek, 31000

    Ivana Jukić, MD, PhD, ivana.jukic@mefos.hr

    Recruiting

Other trials in Croatia

About this study

Official title: Effects of Carnosine Supplementation in Form of Capsules and Functional Food on Cardiovascular Function

Carnosine is a dipeptide synthesized in the body from β-alanine and L-histidine. It was originally discovered in skeletal muscle where it is present in larger amounts than in other tissues, but it is also found in high concentrations in the brain, heart, and gastrointestinal tissues of humans. Although its physiological role has not been completely understood yet, carnosine is a non-enzymatic free-radical scavenger and a natural antioxidant and has anti-inflammatory and neuroprotective properties.

The hypothesis of this research is that the consumption of carnosine supplements in the form of capsules, as well as chicken meat enriched with carnosine (functional food) has a beneficial effect on vascular reactivity measured in different vascular basins, and the lipid profile with a positive effect on the reduction of oxidative stress and inflammatory response in healthy sedentary people. subjects and active athletes measured in different vascular basins.

The main goal of this study is to investigate the influence of carnosine supplement consumption (in the form of capsules and functional food) on vascular and endothelial function in a population of healthy young subjects and active athletes.

Conditions
Carnosine
Being tested
Carnosine supplementation, Controls
Keywords
carnosine, oxidative stress, vascular reactivity, endothelium, inflammation, microcirculation, macrocirculation
Medical subject headings
Inflammation

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Carnosine supplementationDietary supplement

    Intake of carnosine supplement in form of capsules or functionally enriched chicken meet for three weeks

  • ControlsDietary supplement

    Intake of placebo capsules or regular chicken meet for three weeks

Study groups in NCT05723939
Study groupRoleWhat they receive
CarnosineExperimentalIntake of carnosine supplement in form of capsules or functionally enriched chicken meet for three weeks
Receives: Dietary Supplement: Carnosine supplementation
ControlPlacebo comparatorIntake of placebo capsules or regular chicken meet for three weeks
Receives: Dietary Supplement: Controls

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Microvascular endothelial function

    Cutaneous microvascular blood flow will be measured by Laser Doppler Flowmetry in response to vascular occlusion (post occlusive reactive hyperaemia - PORH), in response to iontophoresis of acetylcholine (ACh) and local thermal hyperemia (LTH).

    Measured: 3 weeks

  2. Macrovascular endothelial function

    Measurement of flow mediated dilation (FMD) of brachial artery using ultrasound.

    Measured: 3 weeks

  3. Cerebrovascular reactivity

    Measurement of cerebrovascular blood flow using transcranial color Doppler (TCD).

    Measured: 3 weeks

Secondary outcomes (10)
  1. Lipid profile

    Measurement of plasma cholesterol, HDL cholesterol, LDL cholesterol and triglycerides level.

    Measured: 3 weeks

  2. Oxidative stress status

    Measurement of Thiobarbituric Acid Reactive Substances (TBARS).

    Measured: 3 weeks

  3. Systemic hemodynamics

    Non-invasive assessment of systemic hemodynamics using impedance cardiography (CardioScreen 2000) - SV Stroke Volume (mL).

    Measured: 3 weeks

  4. Serum Pro- and Anti-Inflammatory Cytokines, Chemokines, Growth Factors and Soluble Cell Adhesion Molecules Protein Concentration

    Measurement of serum protein concentration (pg/mL) of various pro- and anti-inflammatory cytokines, chemokines, growth factors and soluble cell adhesion molecules by kits and panels for multiplex protein quantitation using the Luminex 200 instrument platform.

    Measured: 3 weeks

  5. Body composition

    Body composition and body fluid status measurement by a four-terminal portable impedance analyzer. Based on the value of skin resistance (Ohm) empirically derived formulas (the original manufacturer's software) will be used to calculate the estimated Fat Free Mass (FFM kg) and Fat (Fat Mass kg).

    Measured: 3 weeks

  6. Body fluid status

    Body fluid status measurement by a four-terminal portable impedance analyzer. Based on the value of skin resistance (Ohm) empirically derived formulas (the original manufacturer's software) will be used to calculate the estimated Total Body Water (TBW L), Extracellular Water (ECW L), Intracellular Water (ICW L), Plasma Fluid (PF L) and Interstitial Fluid (IF L).

    Measured: 3 weeks

  7. Oxidative stress status

    Measurement of Ferric-Reducing Ability of Plasma (FRAP).

    Measured: 3 weeks

  8. Oxidative stress status

    Measurement of enzyme activity assay of glutathione peroxidase (GPx).

    Measured: 3 weeks

  9. Systemic hemodynamics

    Non-invasive assessment of systemic hemodynamics using impedance cardiography (CardioScreen 2000) - CO Cardiac Output (L/min).

    Measured: 3 weeks

  10. Systemic hemodynamics

    Non-invasive assessment of systemic hemodynamics using impedance cardiography (CardioScreen 2000) - SVRI Systemic Vascular Resistance Index (dyn.s.cm-5 m2).

    Measured: 3 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted13 Feb 2023
  2. Study start1 Sep 2022
  3. Primary completion31 Dec 2023 (estimated)
  4. Study completion30 Jun 2024 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Basic science
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Investigator
Enrolment
100 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05723939
Sponsor's protocol ID
ZCICarnosine
Status last verified
Feb 2023
First submitted
22 Jan 2023
Last updated
14 Feb 2023
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Publications

  • Peric L, Drenjancevic I, Jukic I, Boris A, Susnjara P, Kolobaric N, Mihaljevic Z, Kralik Z, Kralik G, Kosevic M, Galovic O, Stupin A. Carnosine-enriched functional food enhances micro- and macrovascular endothelium-independent vasodilation in competitive athletes-a randomized study. Appl Physiol Nutr Metab. 2025 Jan 1;50:1-11. doi: 10.1139/apnm-2024-0458.

    PubMed 39983097

Questions about this trial

What is this clinical trial studying?

A study testing Carnosine supplementation in people with Carnosine, run by Josip Juraj Strossmayer University of Osijek at 1 site in Croatia.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 14 Feb 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Croatia. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Ines Drenjančević, MD, PhD (+385-31-51-28-00, ines.drenjancevic@mefos.hr), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Microvascular endothelial function (time frame: 3 weeks). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT05723939, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 14 Feb 2023.

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