Online Hemodiafiltration Versus Hemodialysis in Removal of Indoxyl Sulfate in Chronic Hemodialysis Patients

Sponsor
Ain Shams University (Other)
Overall Status
Completed
CT.gov ID
NCT05771350
Collaborator
(none)
60
3
2

Study Details

Study Description

Brief Summary

this study aimed to compare the removal of indoxyl sulphate between hemodiafiltration, high flux hemodialysis and low flux hemodialysis

Condition or Disease Intervention/Treatment Phase
  • Procedure: online hemodiafiltration
  • Procedure: high flux hemodialysis
  • Procedure: low flux hemodialysis
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Hemodiafiltration Versus Hemodialysis in Removal of Indoxyl Sulfate in Chronic Hemodialysis Patients
Actual Study Start Date :
Nov 15, 2016
Actual Primary Completion Date :
Jan 15, 2017
Actual Study Completion Date :
Jan 15, 2017

Arms and Interventions

Arm Intervention/Treatment
Experimental: online hemodiafiltration

Procedure: online hemodiafiltration
20 patients on regular hemodialysis received online hemodiafiltration

Active Comparator: high flux hemodialysis

Procedure: high flux hemodialysis
20 patients on regular hemodialysis received high flux hemodialysis

Active Comparator: low flux hemodialysis

Procedure: low flux hemodialysis
20 patients on regular hemodialysis received low flux hemodialysis

Outcome Measures

Primary Outcome Measures

  1. dialytic removal of indoxyl sulpahte [one month when all samples were collected]

    assessed by the reduction ration of indoxyl sulphate

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • maintenance hemodialysis patients aged more than 18 years
Exclusion Criteria:
  • active illnesses, hospitalization, malignancy

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Ain Shams University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Mohamed sary gharib, Dr, Ain Shams University
ClinicalTrials.gov Identifier:
NCT05771350
Other Study ID Numbers:
  • FMASU MD 301/2016
First Posted:
Mar 16, 2023
Last Update Posted:
Mar 16, 2023
Last Verified:
Mar 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Mar 16, 2023