The Study of Association Between Intradialysis Sodium Balance and Clinical Outcomes in Chronic Hemodialysis Patients

Status

UNKNOWN

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02487004

Enrollment

Registered

2015-07-01

Start date

2015-07-31

Completion date

2016-12-31

Last updated

2015-07-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

End-stage Renal Disease

Brief summary

The purpose of this study is to determine whether the change of serum and dialysate sodium level during hemodialysis can influence on blood pressure and intradialytic weight gain in chronic hemodialysis patients.

Interventions

DEVICEhemodialysis

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

20 Years to No maximum

Healthy volunteers

Inclusion criteria

* age 20 years or more * hemodialysis vintage over 3 months * dialyzed for 4 hours three times per week * hemodialysis adequacy (Kt/V) over 1.2

Exclusion criteria

* diagnosed with chronic hepatitis or infection

Design outcomes

Primary

Measure	Time frame	Description
intradialytic sodium gradient	baseline and 4 hours	change of serum sodium level between initiation and termination of hemodialysis

Countries

South Korea

Contacts

Primary ContactSu Hyun Kim, vice professor

sh76so@cau.ac.kr1800-1114

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026