Effects of Royal Jelly Supplementation in Chronic Kidney Disease
Condition(s) studied
Investigational drug(s) / intervention(s)
Real Jelly: Participants will receive 500mg of royal jelly capsules per day for two months.
Placebo: Participants will receive 500mg of placebo capsules per day for two months.
Study summary
The objective of this study is to evaluate the effects of royal jelly on inflammation and cellular senescence in patients with chronic kidney disease (CKD) on hemodialysis (HD).
Eligibility
Primary outcome measure(s)
- Change in inflammatory biomarkers — 6 weeks
Changes in the mRNA levels of Nrf2, Keap1, Bach1, NLPR3, NF-kB, HO-1, NQO1, p14, p16, p21 and p53 as well as VCAM, ICAM and E-selectin and TLR-4, TNFR and AhR receptors, which will be evaluated from peripheral blood mononuclear cells.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Denise Mafra | Rio de Janeiro | Rio de Janeiro | Recruiting |
More Universidade Federal Fluminense trials in Brazil
Other trials for the same condition
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 NCT06438445 on ClinicalTrials.gov ↗ ← All trials in Brazil