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Recruiting NCT06917131

NCT06917131 Royal Jelly as a Strategy to Modulate Inflammation and Oxidative Stress in Patients With Systemic Arterial Hypertension

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Clinical Trial Summary
NCT ID NCT06917131
Status Recruiting
Phase
Sponsor Universidade Federal Fluminense
Condition Hypertension
Study Type INTERVENTIONAL
Enrollment 34 participants
Start Date 2024-09-18
Primary Completion 2025-08-31

Trial Parameters

Condition Hypertension
Sponsor Universidade Federal Fluminense
Study Type INTERVENTIONAL
Phase N/A
Enrollment 34
Sex ALL
Min Age 18 Years
Max Age 75 Years
Start Date 2024-09-18
Completion 2025-08-31
Interventions
Royal JellyPlacebo

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Brief Summary

The study aims to evaluate the effect of the royal jelly on inflammation and oxidative stress in participants with systemic arterial hypertension. A longitudinal double-blind randomized clinical trial will be carried out, involving hypertensive participants for two months.

Eligibility Criteria

Inclusion Criteria: * patients using one to three antihypertensive medications, undergoing regular follow-up at the HUAP Medical Clinic for more than 6 months and without the need for changes in medication doses in the last 3 months. Exclusion Criteria: * Patients with autoimmune and infectious diseases, diabetes, chronic kidney disease, liver disease, cancer and AIDS will be excluded; pregnant women; those using catabolic drugs or antibiotics; use of antioxidant vitamin supplements, prebiotics, probiotics, symbiotics, habitual intake of royal jelly, and who are allergic to cornstarch or report having an allergy to bee stings will also be excluded. Patients with acute myocardial infarction (AMI) and/or stroke (CVA) in the last 6 months will also be excluded; with HAS stages 2 or 3.

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