Red Propolis Supplementation as a Strategy in Chronic Kidney Disease
Condition(s) studied
Investigational drug(s) / intervention(s)
Red Propolis: Participants will receive 200mg of red propolis capsules per day for two months.
Placebo Control: Participants will receive 200mg of placebo capsules per day for two months.
Study summary
The objective of this study is to evaluate the effects of red propolis on inflammation and oxidative stress in patients with chronic kidney disease on conservative management.
Eligibility
Primary outcome measure(s)
- Change in inflammatory biomarkers — 8 weeks
Changes in the IL-6 and TNF-α
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 NCT07597005 on ClinicalTrials.gov ↗ ← All trials in Brazil