CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 21 enrolled
Drug / intervention
Eleutherococcus senticosus +1 moredietary
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03210519
NCT03210519N/ACompleted

A Randomized, Double-blind, Placebo-controlled Trial to Evaluate the Efficacy of Eleutherococcus Senticosus for Anti-inflammation and Improvement of Erythropoietin Hyporesponsiveness in Subjects Under Renal Dialysis

Chung Shan Medical University·interventional·Posted Jul 7, 2017·Updated Sep 16, 2020

In Brief

A clinical study evaluating Eleutherococcus senticosus and Placebo for Renal Dialysis. Completed, enrolled 21 participants.

Detailed Summary

This is a randomized, double-blind, placebo-controlled, parallel comparison trial to evaluate the efficacy and safety of Eleutherococcus Senticosus taken orally by patients under regular dialysis. Eligible subjects with written consent were randomized into one of the two groups: A. Acanthopanax senticosus (30mg/vial); B. Placebo. After 2-4 weeks of run-in period, the study subjects were asked to take the investigational products orally for 90 days in order to evaluate the effects of oral Eleutherococcus Senticosus liquid on the markers of inflammation, anemia, and safety, and to compare the efficacy among oral Acanthopanax senticosus and placebo.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsRenal Dialysis
Countries--
Collaborators--

Timeline

N/ACompletedFinished
20162017201820192020202120222023202420252026
First PostedJul 7, 2017
Enrollment StartDec 9, 2015
Primary CompletionJun 30, 2017
TodayJul 2, 2026
Enrollment to primary: 1.6 yearsPosted 9.0 years ago

Interventions

Eleutherococcus senticosusdietary

taken orally once/day for 90 days

Placeboother

taken orally once/day for 90 days