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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05840796
Other study ID # TTMHH-103006
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 1, 2014
Est. completion date February 28, 2015

Study information

Verified date April 2023
Source Taipei Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study investigated the beneficial effects of soybean on the renal function, oxidative stress, and inflammatory responses in patients with end-stage diabetic nephropathy (DN).


Description:

DN outpatients were recruited from Tung's Taichung MetroHarbor Hospital (Taichung City, Taiwan). They were randomly separated into two groups; one group was given soy protein drink and the other group was given casein drink for 4 months. The blood pressure, plasma glucose, lipid profile, renal function (estimated glomerular filtration rate, eGFR), inflammatory factor levels were analyzed at the baseline and at the end of the study.


Recruitment information / eligibility

Status Completed
Enrollment 45
Est. completion date February 28, 2015
Est. primary completion date February 28, 2015
Accepts healthy volunteers No
Gender All
Age group 40 Years to 75 Years
Eligibility Inclusion Criteria: - Participants aged from 40 to 75 years and were at DN stage 4 or 5 were enrolled in this study. Exclusion Criteria: - The exclusion criteria were having hemodialysis, lactose intolerance, gastrointestinal (GI) tract dysfunction, liver disease, acute metabolic acidosis or ketoacidosis, in acute infection, severe dehydration, alcohol abuse, addictive drug abuse, cancer in recent 5 years, being involved in another trial in past 1 month, had operation in the past 4 months, or had compliance lower than 90% in the first month of study.

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
soy protein drink
The calories oral nutrition supplements were 100 kcal, which included 8.4g of protein and phosphorous was excluded in two oral nutrition supplements formula. Each participant had two packs of nutrition supplement per day for 4months. The 24-h dietary record, blood pressure, plasma glucose, lipid profile, renal function (estimated glomerular filtration rate, eGFR), inflammatory factor levels were analyzed at the baseline and at the 4th month of the study. The participants were followed up until the 7th month of the study.
casein protein drink
The calories oral nutrition supplements were 100 kcal, which included 8.4g of protein and phosphorous was excluded in two oral nutrition supplements formula. Each participant had two packs of nutrition supplement per day for 4 months. The 24-h dietary record, blood pressure, plasma glucose, lipid profile, renal function (estimated glomerular filtration rate, eGFR), inflammatory factor levels were analyzed at the baseline and at the 4th month of the study. The participants were followed up until the 7th month of the study.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Taipei Medical University

Outcome

Type Measure Description Time frame Safety issue
Primary 24-hours dietary recall Estimated by registered dietitian to understand calories, protein and nutrients intake.. Change from Baseline and 4th and 7th week, the intervention will last for 4 months and follow up for 3 months
Primary estimated glomerular filtration rate (eGFR) renal function Change from Baseline and 4th and 7th week, the intervention will last for 4 months and follow up for 3 months
Primary creatinine renal function Change from Baseline and 4th and 7th week, the intervention will last for 4 months and follow up for 3 months
Primary plasma malondialdehyde (MDA) Antioxidative statement-lipid peroxidation Change from Baseline and 4th and 7th week, the intervention will last for 4 months and follow up for 3 months
Primary high-sensitivity C-reactive protein (hs-CRP) inflammatory indicators Change from Baseline and 4th and 7th week, the intervention will last for 4 months and follow up for 3 months
Primary soluble intercellular adhesion molecule (sICAM)-1 inflammatory indicators Change from Baseline and 4th and 7th week, the intervention will last for 4 months and follow up for 3 months
Primary soluble vascular cell adhesion molecule (sVICAM)-1 inflammatory indicators Change from Baseline and 4th and 7th week, the intervention will last for 4 months and follow up for 3 months
Primary interleukin (IL)-6 inflammatory indicators Change from Baseline and 4th and 7th week, the intervention will last for 4 months and follow up for 3 months
Secondary Blood pressure systolic blood pressure (SBP), diastolic blood pressure (DBP) Change from Baseline and 4th and 7th week, the intervention will last for 4 months and follow up for 3 months
Secondary body weight body weight Change from Baseline and 4th and 7th week, the intervention will last for 4 months and follow up for 3 months
Secondary blood glucose fasting plasma glucose (FPG) Change from Baseline and 4th and 7th week, the intervention will last for 4 months and follow up for 3 months
Secondary lipid profile triglycerides (TG), total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C), and high-density lipoprotein cholesterol (HDL-C) Change from Baseline and 4th and 7th week, the intervention will last for 4 months and follow up for 3 months
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