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Effects of Ingesting Multiple Boluses of Collagen on Muscle & Skin Connective Protein Synthesis in Vivo in Humans (CODIAK)

Maastricht University Medical Centre (MUMC) logo

Maastricht University Medical Centre (MUMC)

Status

Not yet enrolling

Conditions

Muscle Protein Synthesis

Treatments

Dietary Supplement: Collagen protein
Behavioral: Resistance exercise

Study type

Interventional

Funder types

Other

Identifiers

NCT06435637
METC 22-018

Details and patient eligibility

About

Rationale: Collagen protein is the central structural component of extracellular connective tissues within skeletal muscle, bone, cartilage and skin. Dietary collagen peptides are a promising protein source to deliver the specific amino acid precursors required to support an increase in connective tissue protein synthesis across several tissues (e.g. muscle, skin). However, the digestion and absorption kinetics of multiple boluses of collagen peptides and the subsequent impact on muscle and skin connective tissue protein synthesis rates have not yet been assessed in vivo in humans.

Objective: To assess the impact of ingestion of multiple boluses of collagen peptides on muscle connective and skin protein synthesis in vivo in humans.

Study design: Double-blind, parallel-group, placebo-controlled intervention study.

Study population: 20 healthy young males, aged 18-35 years.

Intervention : Participants will perform unilateral resistance exercise followed by the ingestion of either 100 g of collagen peptides (in boluses) or a non-caloric placebo (flavoured water) drinks, while all drinks will contain vitamin C. Continuous intravenous stable isotope amino acid tracer infusions will be applied, plasma, skin and muscle samples will be collected in order to assess protein synthesis rates in skin and muscle tissue.

Main study parameters/endpoints: Primary study parameters are muscle connective protein synthesis rates. Secondary study parameters are skin and myofibrillar protein synthesis rates, plasma amino acid concentrations and body composition.

Enrollment

27 estimated patients

Sex

Male

Ages

18 to 35 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Aged between 18-35 years
  • Male
  • Healthy, recreationally active (participating in recreational sports activities ≥ 1 and ≤ 6 h per week, with a maximum of 2 h resistance-type exercise)
  • 18.5 ≤ BMI ≤ 30 kg/m2
  • No physical limitations (i.e. able to perform all activities associated with daily living in an independent manner).

Exclusion criteria

  • Female
  • Smoking
  • Musculoskeletal disorders
  • Metabolic disorders
  • Use of any medications known to affect protein metabolism (i.e. corticosteroids, non-steroidal anti-inflammatories, or prescribed acne medications).
  • Chronic use of gastric acid suppressing medication or anti-coagulants
  • Unstable weight over the last three months
  • Diagnosed GI tract disorders or diseases
  • Blood donation in the past 2 months

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

27 participants in 2 patient groups, including a placebo group

Collagen protein
Experimental group
Description:
100 g of collagen peptides (in boluses) with vitamin C
Treatment:
Behavioral: Resistance exercise
Dietary Supplement: Collagen protein
Placebo
Placebo Comparator group
Description:
Non-caloric placebo (flavoured water) drinks, with vitamin C.
Treatment:
Behavioral: Resistance exercise

Trial contacts and locations

1

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Central trial contact

Luc JC van Loon, PhD

Data sourced from clinicaltrials.gov

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