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Completed

NCT Number: NCT05330663

Low Protein Renal Formula as Meal Replacement in Predialysis CKD Patients

A high energy and low protein renal formula tailored for the specific needs of pre-dialysis CKD patients.

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Key information

Age range

20 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Taichung Verterans General Hospital Taichung

Taichung, ROC, 40705, Taiwan

About this study

Previous studies indicated that low-protein formula nutritional supplements may improve compliance with an LPD and are beneficial in the management of pre-dialysis CKD patients

This study will evaluate the suitability of the disease-specific enteral formula Fresubin® renal in predialysis chronic kidney disease patients.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Chronic kidney disease stage 4-5 (eGFR <30 mL/min/1.73m2)
  • Age: 20-80 years
  • Patients on low protein diet (0.6-0.8 g protein/kg/d) for at least 3 months
  • Written informed consent

Exclusion criteria

  • Dialysis or planned start of dialysis within next 3 months
  • Patients awaiting kidney transplantation
  • BMI <18 and >30 kg/m2
  • Malnourished patients with albumin levels less than 3 g/dL who need additional supplementation of calories and nutrients
  • Severe liver disease, malignant disease, infectious disease
  • Existing gastrointestinal diseases or pathological findings, which do not allow EN, e.g. intestinal atony, ileus, acute upper GI bleeding, shock, or malabsorption, e.g. inflammatory bowel disease, pancreatic disease, or previous surgical GI resection
  • Severely impaired gastrointestinal function, i.e. severe constipation or acute diarrhea (≥ 3 loose or watery stools per day)
  • Dysphagia or high aspiration risk
  • Relevant CNS and/or psychiatric disorders
  • Known allergic reaction or intolerance to any of the ingredients of the study product
  • Planned surgery or hospitalization during study period
  • Suspicion of drug abuse
  • Patients unable to follow study instructions or keeping a dietary diary
  • Pregnant or lactating women
  • Participation in another clinical trial with an investigational product within 30 days prior to start of study or during the study

Treatment and study plan

Low protein diet with Fresubin® renal

Dietary Supplement

Low protein diet with Fresubin® renal Dosage: 1 bottle per day as a replacement for one regular meal. All patients will get individualized dietary counseling aimed at achieving a protein intake of 0.6-0.8 g/kg actual body weight/day and an energy intake of 30-35 kcal/kg actual body weight.

Low protein diet with normal food

Other

All patients will get individualized dietary counseling aimed at achieving a protein intake of 0.6-0.8 g/kg actual body weight/day and an energy intake of 30-35 kcal/kg actual body weight/day.

Primary outcomes

  1. Change of body weight

    Time frame: baseline to week 4

    Body weight measured in kilograms

Secondary outcomes

  1. Change 3-day dietary record

    Time frame: baseline to week 4

    Total energy intake,3 macronutrients (carbohydrates, protein and lipids) and micronutrients

  2. Change body composition

    Time frame: baseline to week 4

    Body composition measured by bioelectrical impedance analyses

  3. Change of renal fuction

    Time frame: baseline to week 4

    blood urea nitrogen,serum creatinine and estimated glomerular filtration rate

  4. Change of electrolytes

    Time frame: baseline to week 4

    Sodium,potassium,calciam,phosphorus and magnesium in the blood

  5. Safety and compliance.

    Time frame: baseline to week 4

    gastrointestinal symptoms measured by questionnaire

  6. Change in lipid analysis

    Time frame: baseline to week 4

    Change of cholesterol ,triglyceride ,and LDL-cholesterol in the blood

  7. Change of Body Mass Index (BMI) levels

    Time frame: baseline to week 4

    BMI was calculate by body weight (kg) divided by the square of the height (m^2)

  8. Change of waist circumference levels

    Time frame: baseline to week 4

    Waist circumference was measured by a tape

  9. Change of grip strength levels

    Time frame: baseline to week 4

    hand grip strength was measured by grip strength device

  10. Change of CRP

    Time frame: baseline to week 4

    Change of CRP in the blood

  11. Change of nutrition status in blood test

    Time frame: baseline to week 4

    Serum albumin, pre-albumin, total protein, uric acid

  12. Change of daily protein intake

    Time frame: baseline to week 4

    24-hour urine estimated protein intake with Maroni formula

Sponsors and collaborators

Lead sponsor

Taichung Veterans General Hospital

Other

Collaborators

  • Fresenius Kabi Taiwan Ltd.

Registry information

Official study title

High Energy Low Protein Renal Formula as Meal Replacement in Predialysis CKD Patients

Important dates

Study start
2020
Primary completion
2020
Study completion
2020
First posted
Apr 15, 2022
Registry last updated
Apr 15, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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