Long-term Outcome of End-stage Renal Disease Patients Treated With Hig-efficiency Hemodiafiltration

NCT ID: NCT02576873

Last Updated: 2016-07-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

66 participants

Study Classification

OBSERVATIONAL

Study Start Date

2014-03-31

Study Completion Date

2016-03-31

Brief Summary

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A retrospective cohort study was conducted in 66 end-stage renal disease patients who underwent high-efficiency hemodiafiltration technique in King Chulalongkorn Memorial Hospital between 2001-2013 to determine the survival rate as well as other long-term outcome.

Detailed Description

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Growing evidences suggested the superiority of high-efficiency hemodiafiltration (HDF) which could provide both diffusion and convection in a single therapy compared with the conventional hemodialysis. However, the long-term, upto 10 years, outcome still limited. This retrospective cohort study was conducted in 66 end-stage renal disease patients who underwent high-efficiency hemodiafiltration technique in a single-center, King Chulalongkorn Memorial Hospital, between 2001-2013 to determine the survival rate as well as other long-term outcome

Conditions

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End-stage Renal Disease

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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Hemodiafiltration

End-stage renal disease patients who were treated with high-efficiency hemodiafiltration for more than 6 months

Hemodiafiltration

Intervention Type OTHER

Hemodiafiltration treatments were prescribed to the patients as their long-term renal replacement therapies

Interventions

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Hemodiafiltration

Hemodiafiltration treatments were prescribed to the patients as their long-term renal replacement therapies

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Aged 18 years or more
* Be diagnosed end-stage renal disease for more than one year
* Have been regularly received long-term hemodiafiltration for more than 6 months.

Exclusion Criteria

* Patients who received hemodiafiltration less than 6 months
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Chulalongkorn University

OTHER

Sponsor Role lead

Responsible Party

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Khajohn Tiranathanagul

Assistant Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Khajohn Tiranathanagul, MD

Role: PRINCIPAL_INVESTIGATOR

Chulalongkorn University

Locations

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King Chulalongkorn Memorial Hospital

Pathumwan, Bangkok, Thailand

Site Status

Countries

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Thailand

Other Identifiers

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455/56

Identifier Type: -

Identifier Source: org_study_id

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