No phaseRecruiting

Tocotrienol Supplementa as A Senolytic Agent in Middle-aged Adults

A Randomized, Double-Blind, Placebo-Controlled Phase 2 Clinical Trial Evaluating Tocotrienol-Rich Fraction as a Senolytic Agent in Middle-Aged Adults

Sponsor
National University of Malaysia (Academic or other)
Enrolment
220 planned
Conditions
Healthy
Interventions
Treatment; Placebo
Ages
adults
Registry
NCT07637487

From the registry

The goal of this clinical trial is to determine whether tocotrienol works as a senolytic agent to delay age-related biological changes in middle-aged adults. The study will also evaluate the safety of tocotrienol supplementation. The main questions it aims to answer are: Does tocotrienol reduce markers of cellular senescence, inflammation, oxidative stress, and mitochondrial dysfunction? What health changes or medical issues occur in participants taking tocotrienol? Researchers will compare tocotrienol-rich fraction to a placebo (a look-alike capsule with no active ingredient) to determine whether tocotrienol is effective in modulating aging-related pathways. Participants will: Take tocotrienol (200 mg/day) or a placebo daily for 6 months Attend study visits at baseline, 3 months, and 6 months for clinical assessments and laboratory tests Undergo blood sampling and health evaluations, including measures of senescence-associated secretory phenotype (SASP), inflammation, oxidative stress, mitochondrial function, vascular health, skin status, cognitive function, body…

Primary outcomes

  • Blood pressure
  • Changes in Advanced Glycation End Products (AGEs)
  • Changes in Protein Carbonyl
  • Change in Malondialdehyde (MDA)
Full record on ClinicalTrials.gov