The Role of Peritoneal Dialysis in Patients With Refractory Heart Failure and Chronic Kidney Disease
1 other identifier
interventional
7
1 country
1
Brief Summary
In patients with advanced heart failure (HF), systemic congestion is the main indication for hospitalization. Recent evidence has highlighted the role of fluid retention in the pathogenesis of renal dysfunction and subsequent diuretic resistance. Previous kidney disease, diuretic resistance, and progression of renal dysfunction often coexist in patients with HF and persistent volume overload. This clinical presentation represents the most extreme feature of the cardio-renal syndrome. However, available therapeutic options for this ominous condition are scarce and limited. Indeed, there are no data from randomized control trials using pharmacological interventions that support the beneficial effect on survival. Interestingly, intermittent ultrafiltration has recently emerged as an alternative therapeutic option for reducing volume overload in patients with refractory HF. Current literature suggests that it has potential advantages over standard medical treatment particularly in acute stages of HF. Among ultrafiltration methods, peritoneal dialysis (PD) has been preferred as an additional resource for the treatment of advanced congestive heart failure (CHF) compared with hemodialysis because it can provide a more physiological and continuous ultrafiltration. In fact, several studies showed that use of PD improved clinical functional class and hemodynamic parameters and reduced hospitalization rates in patients with CHF. Nevertheless, most studies were limited by retrospective analyses of small sample size, prospective observational design with no control group, or inclusion of patients with end-stage renal failure. Therefore, well-designed prospective randomized controlled studies are mandatory to confirm the effects of PD in these patients.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Dec 2013
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 24, 2012
CompletedFirst Posted
Study publicly available on registry
January 1, 2013
CompletedStudy Start
First participant enrolled
December 1, 2013
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 8, 2015
CompletedStudy Completion
Last participant's last visit for all outcomes
October 8, 2015
CompletedMarch 29, 2019
April 1, 2016
1.9 years
December 24, 2012
March 27, 2019
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Changes of New York Heart Association (NYHA) functional class
at 0 (±1 week), 12 (±1 week), and 24 (±1 week) weeks)
Study Arms (2)
Peritoneal dialysis group
NO INTERVENTIONConventional treatment group
EXPERIMENTALmedical treatment such as diuretics
Interventions
PD exchanges will be customized depending on patient fluid status. At least one daily exchange of icodextrin PD solution will be provided to PD group.
Eligibility Criteria
You may qualify if:
- At least two non-planned admissions for acute heart failure (AHF), the last episode being in the past 6 months
- New York Heart Association (NYHA) functional class III/IV and left ventricular ejection fraction (LVEF) less than 40%
- Persistent congestion despite optimal loop diuretic therapy
- Presence of renal dysfunction \[estimated glomerular filtration rate (eGFR) \< 30 mL/min/1.73 m2\] documented at least once in the last 6 months
You may not qualify if:
- \< 20 years of age
- Pregnancy
- Unsuitable for PD (patients with major abdominal wall defects)
- Allergic to starch or other contraindication to icodextrin (5) End-stage renal disease (eGFR \< 10 ml/min/1.73 m2) requring dialysis treatment
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Division of Nephrology, Department of Internal Medicine Yonsei University College of Medicine
Seoul, 120-752, South Korea
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 24, 2012
First Posted
January 1, 2013
Study Start
December 1, 2013
Primary Completion
October 8, 2015
Study Completion
October 8, 2015
Last Updated
March 29, 2019
Record last verified: 2016-04