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Developing a Nutritional Supplement to Increase Collagen Synthesis in People

University of California (UC) Davis logo

University of California (UC) Davis

Status

Enrolling

Conditions

Exercise
Connective Tissue
Dietary Supplements

Treatments

Dietary Supplement: Natural Product Supplement
Dietary Supplement: Placebo control

Study type

Interventional

Funder types

Other

Identifiers

NCT06138106
2110494

Details and patient eligibility

About

The purpose of this study is to test whether a natural product supplement can potentiate the increase in collagen synthesis following the ingestion of collagen protein. The investigators have developed a model of natural (GRAS certified) products that stimulate collagen synthesis, in vitro. The investigators will determine whether the natural product supplement can potentiate the collagen synthetic response to the ingestion of collagen protein. Basal and fed serum will be isolated and these samples will be used to treat human engineered ligaments.

Enrollment

20 estimated patients

Sex

All

Ages

18 to 30 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Young healthy adults (18-30 y)

Exclusion criteria

  • Pregnancy
  • Smoking
  • Receiving any medication that may interfere with the study outcomes

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Triple Blind

20 participants in 2 patient groups, including a placebo group

Natural Product Supplement
Experimental group
Description:
The participant will consume a dose of hydrolyzed collagen (20g) supplemented with vitamin C (100 mg), epicatechin (75 mg), vitamin E (350 iU) and stevia extract (225 mg).
Treatment:
Dietary Supplement: Natural Product Supplement
Placebo
Placebo Comparator group
Description:
The participant will consume a dose of hydrolyzed collagen (20g) supplemented with vitamin C (100 mg) and sweetener.
Treatment:
Dietary Supplement: Placebo control

Trial contacts and locations

1

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Central trial contact

Kevin Paulussen, PhD; Keith Baar, PhD

Data sourced from clinicaltrials.gov

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