Ireland
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Recruiting Not applicable

Red Propolis Supplementation as a Strategy in Chronic Kidney Disease

NCT07597005 · tracked via the Priya Life Science Brazil tracker
Phase
Not applicable
Started
2025-09-30
Last updated
2026-05-19

Condition(s) studied

Kidney DiseaseOxidative StressChronic Kidney DiseaseInflammation

Investigational drug(s) / intervention(s)

Red PropolisPlacebo Control

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

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * patients with CKD stages 3-5 under conservative management Exclusion Criteria: * pregnant, * lactating, * smoker * patients using antibiotics and antioxidant supplements in the last three months * patients with autoimmune and infectious diseases, * patients with cancer, liver disease, and AIDS

Primary outcome measure(s)

  • Change in inflammatory biomarkers — 8 weeks
    Changes in the IL-6 and TNF-α

Trial sites (1)

FacilityCityRegionStatus
Denise Mafra Rio de Janeiro Rio de Janeiro Recruiting
Official registry record

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