ClinicalTrials.Veeva

Menu

The Effect of Probiotics on Depression Syndrome and Risk Factors of Cardiovascular Disease in Hemodialysis Patients

C

China Medical University

Status and phase

Completed
Phase 4

Conditions

Depression Mild
Cardiovascular Diseases

Treatments

Drug: MIYAIRI 588

Study type

Interventional

Funder types

Other

Identifiers

NCT05724511
CMUH111-REC3-178

Details and patient eligibility

About

As the investigators know, only few researches focus on the effect of probiotics on depression in hemodialysis patients. Besides, probiotics also have benefit effect on dyslipidemia and hypertension in general population. Both of them are the risk factors of cardiovascular disease which is the major cause of death in hemodialysis patients. Therefore, this study looks for the effect of probiotics on depression syndrome and risk factors of cardiovascular disease in hemodialysis patients. This is a randomized controlled trial. All patients will be assigned at random to intervention group or control group. This study plans to recruit 70 hemodialysis patients and expects at least 30 patients in each group at the end of study period. The investigators provide probiotics (C. butyricum MIYAIRI 588) to intervention group and provide nothing to the control group.

All patients need to maintain the lifestyle during study period. Genomic analysis of gut microbiota on patients' fecal samples will be used to evaluation their compliance.

Enrollment

55 patients

Sex

All

Ages

20+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adults aged 20 years or older undergoing hemodialysis (at least 3 months), 3 times per week, and URR ≥65%

Exclusion criteria

  1. allergic to the components of the intervention drug, low tolerance of milk or dairy products
  2. Has the diagnosis of dementia, delirium, bipolar disorder, schizophrenia, or liver failure
  3. Beck Depression Inventory Chinese version 2.0 score higher than 14, or has significant suicide risk during study
  4. Following significantly clinical syndrome: obsessive compulsive disorder, schizoid personality disorder, schizotypal personality, paranoid、antisocial Personality Disorder, histrionic personality disorder
  5. With addiction to alcohol or drugs, terminal cancer, severe infection, heart failure, central venous catheter in the past 6 months
  6. Taking antibiotics, anti-oxidant vitamin supplement, probiotics, prebiotics, antidepressants, anti-anxiety medicine, yogurt and the products in the past 3 months
  7. Pregnant or lactating

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

55 participants in 2 patient groups

Intervention
Experimental group
Treatment:
Drug: MIYAIRI 588
Control
No Intervention group

Trial contacts and locations

1

Loading...

Central trial contact

PEIYU WU

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems