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Clinical Trials in the UK / NCT06603194
Recruiting Not applicable

Benefit of Bovine or Marine Collagen Vs. Placebo on Skin, Hair, Nails and Whole Body Health in Healthy Adults

NCT06603194 · tracked via the Priya Life Science UK tracker
Sponsor
Ancient + Brave
Phase
Not applicable
Started
2024-08-26
Last updated
2024-09-19

Condition(s) studied

Skin LaxityHair ThinningNails

Investigational drug(s) / intervention(s)

Bovine or Marine Collagen

Bovine or Marine Collagen: Bovine or Marine Collagen

Study summary

The BECOME Study (Bovine and Marine Collagen Efficacy for Skin, Hair, Nails and Whole Body Health Markers Evaluation) is a randomized controlled trial designed to compare the effects of bovine and marine collagen supplements versus a placebo on skin, hair, nails and whole body health markers. The trial aims to determine the most efficacious collagen source for improving health outcomes and to establish if both types of collagen are equally effective. Participants will be assessed on various health parameters, including skin elasticity, joint health, digestive health, and overall well-being, over a specified period.

Eligibility

Sex
FEMALE
Min age
35 Years
Max age
55 Years
Healthy volunteers
Accepted
Inclusion Criteria: Females aged 35-55 years. Participants must be comfortable with bovine or marine collagen (non-vegan/vegetarian). Must provide informed consent and be willing to comply with study requirements. Exclusion Criteria: Pregnant or breastfeeding women. History of chronic skin conditions (e.g., eczema, psoriasis) that might interfere with study outcomes. Any active skin infections or severe acne. Currently taking collagen supplements or have taken them within the last 6 months. Use of medications or topical agents that can affect skin, hair, nails, or gastrointestinal health (e.g., corticosteroids, retinoids). Excessive alcohol consumption or current smokers. Regular use of sunbeds. Recent cosmetic procedures (e.g., Botox, fillers, chemical peels, laser treatments) on skin, hair, or nails within the last 3 months. Any condition or situation that, in the opinion of the investigator, may interfere with the participant's ability to comply with the study requirements or give informed consent. Poor adherence to previous study protocols

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Princeton Consumer Research, 8 Richmond Road, Dukes Park Chelmsford Essex Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06603194 on ClinicalTrials.gov ↗ ← All trials in the UK