RiboCeine GSH Clinical Trial

This is a summary of a human clinical trial that concluded in April 2024 concerning the efficacy of RiboCeine (d-ribose-l-cysteine) for raising glutathione in the body.

What You Need to Know

Study Title:

Effect of D-Ribose L-Cysteine (RiboseCysteine) on oxidative stress markers and glutathione levels in healthy individuals aged 38 – 60

Study Facts:

  • Double-blind Placebo Controlled Study
  • Study protocol approved by the University of Santa Catarina (UNISUL) Ethics Committee (Protocol #6.597.558) (2023)
  • All participants were healthy individuals
  • RiboCeine 250 mg (MaxOne) per day versus Placebo
  • Each participant followed the protocol for 28 days; but each had a different start date.
  • Study start: 2023-11-01
  • Experiment end: 2024-03-27
  • Report Delivery: April 2024

General Objectives:

Investigate the effect of RiboseCysteine on serum markers of oxidative stress, inflammation and subjective measures of health.

Objective Measures:

  • Total Serum Glutathione Levels
  • Oxidative Stress Markers
  • Mitochondrial Function
  • Serum Inflammatory and Anti-inflammatory Cytokines

Results Summary:

  • Age 38-60 full group: 26.6% Increase in Serum Glutathione levels versus the Placebo group
  • Age 35-50 sub-group: 16.5% Increase in Serum Glutathione levels
  • Age 51-60 sub-group: 64.7% Increase in Serum Glutathione levels
  • No Negative Side Effects
  • Improved blood flow to the prefrontal cortex
  • Improved heart variability measurements, including heart rate
  • Decreased fat mass
  • Serum markers of oxidative stress and inflammation showed improvements relative to the Placebo group

To see a Press Release from the independent firm that conducted the study go here: RiboCeine Clinical Trial Press Release