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Not Yet RecruitingNCT07296146

Probiotics Against Erythropoietin Resistance in Chronic Kidney Disease Patients.

Effect of Probiotic Supplementation on Resistant Anaemia to Erythropoietin in Chronic Kidney Disease Patients.

Status
Not Yet Recruiting
Phase
Phase 3
Study type
Interventional
Enrollment
80 (estimated)
Sponsor
Badr University · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The goal of this clinical trial is to assess whether probiotic supplementation can improve the hematological response of CKD patients to erythropoietin therapy and prevent or reduce erythropoietin resistance. The main questions it aims to answer are: Can probiotic be used as an adjuvant strategy in anemia management and increasing ESA responsiveness in CKD? What medical problems do participants have when taking probiotic? Researchers will compare Erythropoietin only with Erythropoietin + Probiotic to see if Probiotic aids in treating anaemic chronic kidney disease patients. Participants will: Take Erythropoietin + Probiotic or Probiotic only every day for 3 months Visit the clinic once every 4 weeks for checkups and tests Keep a diary of their symptoms

Conditions

Interventions

TypeNameDescription
DRUGErythropoietin + ProbioticAnaemic chronic kidney disease patients on regular hemodialysis treated with Erythropoietin + Probiotic
DRUGEPOAnaemic chronic kidney disease patients on regular hemodialysis treated with Erythropoietin

Timeline

Start date
2025-12-15
Primary completion
2026-03-15
Completion
2026-05-15
First posted
2025-12-22
Last updated
2025-12-22

Source: ClinicalTrials.gov record NCT07296146. Inclusion in this directory is not an endorsement.