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)