ClinicalTrials.Veeva

Menu

Retrospective Survey of Hyperkalemia in Hemodialysis (Visualize-HD)

P

Peking University

Status

Unknown

Conditions

Hemodialysis Complication

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT05020717
20-20591

Details and patient eligibility

About

This study aim to describe hyperkalemia clinical burden and investigate the risk factors associated with the burden on HD facility level.

Full description

This study is an observational survey study. We estimate 300 hemodialysis (HD) centres will be enrolled in the study. Summarized data on serum potassium (sK) after long interdialytic interval (LIDI), facility practice pattern and patient characteristics which may be related with sK management, and death records information including number of deaths for each centre will be collected. All the data collected and analysed are on HD facility level, not on patient-level. We are aiming to describe hyperkalemia clinical burden and investigate the risk factors associated with the burden on HD facility level. Association between sK management and long-term outcome will also be explored.

Enrollment

300 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

For HD centers:

  • ≥ 100 patients under MHD within 3 years prior the study initiation
  • Willing to participate in the study
  • Have routine blood collection after LIDI
  • Have death records

For HD patients:

• On chronic HD for ≥ 3 months

Exclusion criteria

  • Blood test on other days than those after LIDI
  • Unable to provide detailed data required by study protocol
  • Being unable to comply with study-specified procedure

Trial contacts and locations

1

Loading...

Central trial contact

Xinju Zhao; Li Zuo

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems