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Effect of Dietary Fiber on Non-dialysis Patients With Chronic Kidney Disease

Effect of Dietary Fiber on Anemia and Glomerular Filtration Rate in Non-dialysis Patients With Chronic Kidney Disease

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05835648
Enrollment
56
Registered
2023-04-28
Start date
2023-04-30
Completion date
2024-04-30
Last updated
2023-04-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Kidney Disease

Keywords

Dietary fiber, CKD, Anemia, glomerular filtration rate

Brief summary

The main objective of this study was to investigate the effect of dietary fiber on anemia and glomerular filtration rate in non-dialysis patients with chronic kidney disease. Participants will be randomly divided into a dietary fiber intervention group and a blank control group. The patients in the dietary fiber intervention group will have dietary fiber intake survey conducted by dietitians on the basis of basic treatment. Supplemented dietary fiber was given on the basis of daily diet, once a day, 1 piece each time, before meals, and the intervention lasted for 3 months. The blank control group was followed up without intervention. Clinical data, blood, urine and stool samples were collected at the initial diagnosis and at each follow-up site.

Interventions

DIETARY_SUPPLEMENTNutrasumma

On the basis of daily diet, dietary fiber supplement (Nutrasumma) was given once a day, 1 strip each time, before meals, and the intervention lasted for 3 months.

Sponsors

Qianfoshan Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Above 18 years old; * Clinically confirmed (history, blood creatinine, kidney B-ultrasound, laboratory examination, etc.) as stage 3-5 chronic kidney disease, endogenous creatinine clearance was \< 60ml/min according to Cockcroft-Gault formula; * Generally in good condition, have a good understanding of their own illness and physical condition, have self-awareness, and can communicate well with others; * Hemoglobin 100-130g/L; * In a non-dialysis state. * Dietary fiber intake \<25g/d; * Voluntarily join the study, understand the significance of the test and the indicators to be measured, and sign the informed consent.

Exclusion criteria

* Unwilling to join the study; Severe infection: fever, cough and sputum, pharyngeal pain, abdominal pain, diarrhea, carbuncle and other skin and soft tissue infection and other clinical manifestations, blood routine white blood cell count beyond the normal range (10×109/L); * Severe cardiovascular diseases: including chronic cardiac insufficiency grade 3 or above and various arrhythmias; * Obvious hypoproteinemia: albumin less than 30g/L; * Corrective measures for anemia (blood transfusion, erythropoietin, HIF-PHI, iron supplement) have been applied in the past 3 months; * Tumor evidence: certain tumors have been detected or clinical manifestations and tumor markers suggest the possibility of tumor; * Pregnant women; * Recent history of heavy blood loss.

Design outcomes

Primary

MeasureTime frame
Changes in baseline hemoglobin levels at 9 months9 months
Changes of glomerular filtration rate at baseline at 9 months9 months

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026