Clinical Trials in Brazil / NCT05183737
Active, not recruiting Not applicable

Effects of Microencapsulated Propolis and Turmeric in Patients With Chronic Kidney Disease

NCT05183737 · tracked via the Priya Life Science Brazil tracker
Phase
Not applicable
Started
2022-03-07
Last updated
2025-04-03

Condition(s) studied

Chronic Kidney DiseasesInflammation

Investigational drug(s) / intervention(s)

Microcapsules with turmeric and propolis

Microcapsules with turmeric and propolis: Participants will receive microcapsules containing 0.250 milligrams of turmeric 95% curcumin and 0.250 milligrams of green propolis, twice a day for 12 weeks

Study summary

Oxidative stress and inflammation are correlated with Chronic Kidney Disease (CKD), in a way that they bring several harms to patients, including an increased risk of cardiovascular disease and mortality. Adjuvant therapeutic options such as bioactive compounds present in some foods seem to mitigate inflammation. Turmeric and propolis are foods that have compounds with antioxidant and anti-inflammatory capacity, as they promote the activation of nuclear erythroid transcription factor 2 (Nrf2 - responsible for the synthesis of antioxidant enzymes) and inhibit the activity of nuclear factor Kappa B (NF-κB - which increases the synthesis of inflammatory cytokines). This work aims to evaluate the effects of supplementation of associated propolis and turmeric microcapsules on inflammatory markers in patients with CKD undergoing hemodialysis (HD).

Eligibility

Sex
ALL
Min age
18 Years
Max age
60 Years
Healthy volunteers
No
Inclusion Criteria: * Patients with stage 5 CKD (GFR \< 15 mL/min); * On hemodialysis for more than 6 months; * Who have arteriovenous fistula (AVF) as vascular access Exclusion Criteria: * Pregnant women; * Smokers; * Using antibiotics in the last 3 months; * Using antioxidant supplements; * Who have habitual intake of propolis, curcumin and turmeric; * With autoimmune and infectious diseases, cancer, liver and AIDS (Acquired Immunodeficiency Syndrome)

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Denise Mafra Rio de Janeiro Rio de Janeiro

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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 NCT05183737 on ClinicalTrials.gov ↗ ← All trials in Brazil