Actively Recruiting

Phase Not Applicable
Age: 65Years +
All Genders
NCT06975995

Effect of the Postbiotics on Complications Treatment in Elderly Hemodialysis Patients

Led by Peking University First Hospital · Updated on 2025-05-16

60

Participants Needed

1

Research Sites

121 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of the trial is to explore the effect of exogenous postbiotics supply on the quality of life and nutritional status of elderly hemodialysis patients. Participants will be devided into intervention group and placebo group in an 1:1 ratio.They will: 1. In the treatment period for 12 weeks, intervention group receives postbiotics product while the other group receives placebo. 2. In the subsequent 12 weeks, intervention group ends the trial and placebo group enters into remedial treatment period. Placebo group will receive postbiotics product for 12 weeks. Researchers will analyze the change of indicators such as quality of life and nutrition state of participants from the baseline to end of treatment, and compare the difference between the two group.

CONDITIONS

Official Title

Effect of the Postbiotics on Complications Treatment in Elderly Hemodialysis Patients

Who Can Participate

Age: 65Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 65 years or older
  • Receiving maintenance hemodialysis therapy for at least 6 months
Not Eligible

You will not qualify if you...

  • Medical history affecting oral feeding within the last month (e.g., intestinal obstruction, gastrointestinal bleeding, acute pancreatitis, accidental inhalation)
  • Medical history affecting gastrointestinal functions (e.g., inflammatory bowel disease, irritable bowel syndrome, short bowel syndrome)
  • Inability to communicate and cooperate normally

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

Peking UFH

Beijing, Beijing Municipality, China, 100034

Actively Recruiting

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Research Team

Y

Yuqing Chen

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

TREATMENT

Number of Arms

2

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