Clinical Trials Directory

Trials / Unknown

UnknownNCT05227313

Double-Blind, Placebo-Controlled Trial of Eefooton in Patients With Chronic Kidney Disease

Evaluation Dietary Supplement" Eefooton" on the Quality of Life in Chronic Kidney Disease

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
120 (estimated)
Sponsor
Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation · Academic / Other
Sex
All
Age
20 Years – 85 Years
Healthy volunteers
Not accepted

Summary

This phase II study, 24-week, double-blind, study evaluated Eefooton's safety and efficacy for patients with CKD stage 3 to 4 Not on dialysis.

Detailed description

The purpose of this clinical observation and research is to evaluate the eGFR changes in the renal function of patients with chronic kidney disease combination the Eefooton oral solution and commonly used chemical drugs.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTEefooton oral solutionEefooton is extracted from Rhodiola, Huang Qi, American Ginseng, Dang Ginseng, and Ligustrum lucidum by biotechnology. It has immunomodulatory effects, anti-oxidation and anti-inflammatory effects, and regulates calcium metabolism.
DIETARY_SUPPLEMENTPlacebo oral solutionoral solution matched placebo

Timeline

Start date
2022-03-01
Primary completion
2024-12-31
Completion
2024-12-31
First posted
2022-02-07
Last updated
2022-03-02

Locations

1 site across 1 country: Taiwan

Source: ClinicalTrials.gov record NCT05227313. Inclusion in this directory is not an endorsement.