To Explore the Anti-oxidative Effects and Inflammation Effects of Soy Protein to Renal Function of End Stage Diabetes Nephropathy Patients

Sponsor
Taipei Medical University (Other)
Overall Status
Completed
CT.gov ID
NCT05840796
Collaborator
(none)
45
2
10.9

Study Details

Study Description

Brief 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).

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: soy protein drink
  • Dietary Supplement: casein protein drink
N/A

Detailed 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.

Study Design

Study Type:
Interventional
Actual Enrollment :
45 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Actual Study Start Date :
Apr 1, 2014
Actual Primary Completion Date :
Feb 28, 2015
Actual Study Completion Date :
Feb 28, 2015

Arms and Interventions

Arm Intervention/Treatment
Experimental: 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.

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.

Other: 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.

Dietary Supplement: 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.

Outcome Measures

Primary Outcome Measures

  1. 24-hours dietary recall [Change from Baseline and 4th and 7th week, the intervention will last for 4 months and follow up for 3 months]

    Estimated by registered dietitian to understand calories, protein and nutrients intake..

  2. estimated glomerular filtration rate (eGFR) [Change from Baseline and 4th and 7th week, the intervention will last for 4 months and follow up for 3 months]

    renal function

  3. creatinine [Change from Baseline and 4th and 7th week, the intervention will last for 4 months and follow up for 3 months]

    renal function

  4. plasma malondialdehyde (MDA) [Change from Baseline and 4th and 7th week, the intervention will last for 4 months and follow up for 3 months]

    Antioxidative statement-lipid peroxidation

  5. high-sensitivity C-reactive protein (hs-CRP) [Change from Baseline and 4th and 7th week, the intervention will last for 4 months and follow up for 3 months]

    inflammatory indicators

  6. soluble intercellular adhesion molecule (sICAM)-1 [Change from Baseline and 4th and 7th week, the intervention will last for 4 months and follow up for 3 months]

    inflammatory indicators

  7. soluble vascular cell adhesion molecule (sVICAM)-1 [Change from Baseline and 4th and 7th week, the intervention will last for 4 months and follow up for 3 months]

    inflammatory indicators

  8. interleukin (IL)-6 [Change from Baseline and 4th and 7th week, the intervention will last for 4 months and follow up for 3 months]

    inflammatory indicators

Secondary Outcome Measures

  1. Blood pressure [Change from Baseline and 4th and 7th week, the intervention will last for 4 months and follow up for 3 months]

    systolic blood pressure (SBP), diastolic blood pressure (DBP)

  2. body weight [Change from Baseline and 4th and 7th week, the intervention will last for 4 months and follow up for 3 months]

    body weight

  3. blood glucose [Change from Baseline and 4th and 7th week, the intervention will last for 4 months and follow up for 3 months]

    fasting plasma glucose (FPG)

  4. lipid profile [Change from Baseline and 4th and 7th week, the intervention will last for 4 months and follow up for 3 months]

    triglycerides (TG), total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C), and high-density lipoprotein cholesterol (HDL-C)

Eligibility Criteria

Criteria

Ages Eligible for Study:
40 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Taipei Medical University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Taipei Medical University
ClinicalTrials.gov Identifier:
NCT05840796
Other Study ID Numbers:
  • TTMHH-103006
First Posted:
May 3, 2023
Last Update Posted:
May 3, 2023
Last Verified:
Apr 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 3, 2023