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Clinical Trials/NCT03385902
NCT03385902
Unknown
Not Applicable

Impact on Mortality of Timing of Dialysis Initiation in Patients With End-stage Renal Disease by a Novel Assessment Based on Fuzzy Mathematics

The First Affiliated Hospital of Dalian Medical University1 site in 1 country388 target enrollmentApril 14, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Chronic Kidney Disease
Sponsor
The First Affiliated Hospital of Dalian Medical University
Enrollment
388
Locations
1
Primary Endpoint
cerebro-cardiovascular mortality
Last Updated
4 years ago

Overview

Brief Summary

The purpose of this study is to evaluate the impact of the optimal and late initiation of dialysis on the mortality and quality of life in end-stage renal disease (ESRD) patients by the Dialysis Initiation based on Fuzzy mathematics Equation (DIFE), which is a novel equation for the assessment of timing of dialysis initiation established by Fuzzy mathematics.

Detailed Description

The optimal time of dialysis initiation is still controversial. Estimated glomerular filtration rate (eGFR) which is now widely used as the assessment of timing of dialysis is lack of specificity. Some clinical factors such as heart failure, volume overload, malnutrition also determine the dialysis time. But these subjective judgements do not have a standard. So there is no quantitative assessment of timing of dialysis initiation. The research team developed a novel equation named DIFE (Dialysis Initiation based on Fuzzy mathematics Equation) with data from a retrospective multicenter cohort by fuzzy mathematical methods to combine these clinical factors and lab indexes. The DIFE was confirmed to be more accurate and convenient to use in clinical practice than eGFR only at the assessment of dialysis initiation time in the internal validation. For further validation of the DIFE, the team will conduct a multicenter randomized controlled trial. Patients who need hemodialysis will be randomized to optimal start dailysis group or late start dailysis group by the assessment of the DIFE. Based on the comparison of the two groups, this trial will provide evidence for the optimal timing of dialysis initiation in patients with end-stage renal disease by the DIFE.

Registry
clinicaltrials.gov
Start Date
April 14, 2018
End Date
December 14, 2023
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
The First Affiliated Hospital of Dalian Medical University
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Have progressive chronic kidney disease with an eGFR less than 15 ml/min/1.73m2 and a DIFE between 30-35
  • Expected to commence maintenance hemodialysis as their renal replacement treatment
  • Agreeable to randomization

Exclusion Criteria

  • Acute kidney injury (AKI) or AKI on chronic kidney disease (CKD)
  • With the primary disease of systemic lupus erythematosus (SLE) or systemic vasculitis
  • Have received or planning to receive a kidney transplant or peritoneal dialysis during the study
  • Has a recently diagnosed cancer that was likely to affect survival (except for the following cases: the cancer has been confirmed to be cured or relieved for over 5 years, have had the radical resection for the basal cell carcinoma or squamous carcinoma of skin or carcinoma in-situ of any part of the body )
  • Hepatocirrhosis
  • Positive test of Human Immunodeficiency Virus (HIV), the hepatitis B virus antigen (HBsAg) or anti-hepatitis C virus antibody (HCV Ab)
  • Acute infection within 1 month
  • Bad habit which is difficult to withdrawal such as alcohol abuse
  • Poor compliance and could not be treated according to the protocol
  • Being pregnant, nursing or having a plan for pregnancy

Outcomes

Primary Outcomes

cerebro-cardiovascular mortality

Time Frame: 3 years, from the date of enrollment until the end of study

proportion of patients who die from cerebro-cardiovascular disease

all-cause mortality

Time Frame: from the date of enrollment until the end of study, assessed up to 3 years

proportion of patients who die from any cause

Secondary Outcomes

  • Nutrition assessment(from the date of enrollment until the date of death from any cause, or the end of study, which ever came first, assessed up to 3 years)
  • the change of quality of life(from the date of enrollment until the date of death from any cause, or the end of study, which ever came first, assessed up to 3 years)
  • cognitive dysfunction(from the date of enrollment until the date of death from any cause, or the end of study, which ever came first, assessed up to 3 years)
  • hospitalization(from the date of enrollment until the date of death from any cause, or the end of study, which ever came first, assessed up to 3 years)
  • cerebro-cardiovascular events(from the date of enrollment until the date of death from any cause, or the end of study, which ever came first, assessed up to 3 years)
  • Medical cost(from the date of enrollment until the date of death from any cause, or the end of study, which ever came first, assessed up to 3 years)
  • Hemodialysis complications(from the date of enrollment until the date of death from any cause, or the end of study, which ever came first, assessed up to 3 years)

Study Sites (1)

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