NCT01758627

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
7

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Dec 2013

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 24, 2012

Completed
8 days until next milestone

First Posted

Study publicly available on registry

January 1, 2013

Completed
11 months until next milestone

Study Start

First participant enrolled

December 1, 2013

Completed
1.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 8, 2015

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 8, 2015

Completed
Last Updated

March 29, 2019

Status Verified

April 1, 2016

Enrollment Period

1.9 years

First QC Date

December 24, 2012

Last Update Submit

March 27, 2019

Conditions

Keywords

Peritoneal dialysis,chronic kidney disease,refractory heart failure

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 INTERVENTION

Conventional treatment group

EXPERIMENTAL

medical treatment such as diuretics

Drug: Peritoneal dialysis (PD)

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.

Also known as: 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.
Conventional treatment group

Eligibility Criteria

Age20 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

MeSH Terms

Conditions

Heart FailureRenal Insufficiency, Chronic

Interventions

Peritoneal Dialysis

Condition Hierarchy (Ancestors)

Heart DiseasesCardiovascular DiseasesRenal InsufficiencyKidney DiseasesUrologic DiseasesFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesMale Urogenital DiseasesChronic DiseaseDisease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Renal DialysisRenal Replacement TherapyTherapeuticsSorption Detoxification

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

Locations