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Loop Diuretic Dosage in Patients With Acute Heart Failure and Renal Failure: Conventional Versus Carbohydrate Antigen 125-guided Therapy (IMPROVE-HF) (IMPROVE-HF)

Primary Purpose

Heart Failure

Status
Completed
Phase
Phase 4
Locations
Spain
Study Type
Interventional
Intervention
CA125 guided strategy
CA125 guided strategy
Conventional Strategy
Sponsored by
Fundación para la Investigación del Hospital Clínico de Valencia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Heart Failure focused on measuring Heart Failure, Renal Failure, Biomarker guided-therapy, Loop diuretics, Carbohydrate antigen 125

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Patients with the diagnosis of acute heart failure (AHF) and the concurrence of the following conditions:

  1. Presence of symptoms (dyspnea at rest or minimal exertion) and signs attributable to congestion (signs of congestion on chest radiography, or presence of peripheral edema or ascites, or jugular venous distension at 45 degrees or presence of crackles on auscultation).
  2. Elevated natriuretic peptide (NT-proBNP> 1000 pg/ml or BNP> 100 mg/dl).
  3. Creatinine ≥1,4 mg/dl on admission, provided that the estimated glomerular filtration rate less than 60 ml / min / m2.
  4. Intent to be treated with loop diuretics intravenously.

Exclusion Criteria:

  1. Life expectancy less than 6 months of life due to other comorbid conditions.
  2. Cardiogenic shock.
  3. Diagnosis of acute coronary syndrome in the previous 30 days.
  4. Pregnancy at the time of inclusion.
  5. Restrictive or Obstructive pulmonary disease or severe degree.
  6. Chronic renal insufficiency in stage V (estimated glomerular filtration rate <15 ml / min / m2) or patient previously included in known dialysis program.
  7. Participation in another clinical trial randomized at the time of inclusion.
  8. Temperature ≥38 ° C or diagnosis of pneumonia.

Sites / Locations

  • Hospital Clínico Universitario de Valencia

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

CA125 guided strategy

Conventional strategy

Arm Description

In this group loop diuretic (Furosemide) dosage will be guided by Carbohydrate Antigen 125 (CA125) plasma levels

Standard treatment strategy Therapy is based on established european guidelines

Outcomes

Primary Outcome Measures

Change in renal function (GFR)
Glomerular filtration rate (GFR) estimated by MDRD. Prespecified interim analysis of primary outcome will be made by protocol when first 100 patients are included.

Secondary Outcome Measures

Improvement in signs and symptoms of heart failure (NYHA)
Evaluation of dyspnea (changes in the functional class of the New York Heart Association -NYHA)
Improvement in signs and symptoms of heart failure (VAS)
Evaluation of signs of systemic congestion, and patient global assessment (by visual analogue scale -VAS-)
Changes in plasma levels of natriuretic peptide (NT-proBNP)
Changes in plasma levels of high sensitive troponin
Time required to change intravenous diuretics to oral administration.
Composite of all-cause mortality plus acute heart failure related rehospitalization
Number of events in each group during 30-day follow-up
Change in renal function (creatinin)
Serum levels of creatinine
Change in renal function (urea)
Serum levels of urea
Change in renal function (cystatin C)
Serum levels of Cystatin C

Full Information

First Posted
December 14, 2015
Last Updated
February 11, 2018
Sponsor
Fundación para la Investigación del Hospital Clínico de Valencia
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1. Study Identification

Unique Protocol Identification Number
NCT02643147
Brief Title
Loop Diuretic Dosage in Patients With Acute Heart Failure and Renal Failure: Conventional Versus Carbohydrate Antigen 125-guided Therapy (IMPROVE-HF)
Acronym
IMPROVE-HF
Official Title
Loop Diuretic Dosage in Patients With Acute Heart Failure and Renal Failure: Conventional Versus Carbohydrate Antigen 125-guided Therapy (IMPROVE-HF)
Study Type
Interventional

2. Study Status

Record Verification Date
February 2018
Overall Recruitment Status
Completed
Study Start Date
January 2015 (Actual)
Primary Completion Date
January 30, 2017 (Actual)
Study Completion Date
January 30, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Fundación para la Investigación del Hospital Clínico de Valencia

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Worsening renal function (WRF) is a frequent finding in patients with decompensated acute heart failure (AHF) and it is associated to increased length of hospitalization and higher morbidity and mortality. Traditionally, WRF in AHF setting has been attributed to low cardiac output, but recent evidence also suggests venous congestion play a crucial role. Loop diuretics are the mainstay treatment of AHF, but their use traditionally has been associated to WRF, but also renal function improvement in patients with unequivocal signs of congestion. Nevertheless, traditional symptoms or signs of patients with AHF have shown a limited accuracy to neither identify nor quantify the degree of venous congestion. Recent authors have reported that plasma levels of antigen carbohydrate 125 (CA125) are closely related to the degree of venous congestion. The investigators hypothesize that CA125 may have a role for identifying the hyperhydrated (High CA125) patients that need high loop diuretic doses, and those with normal CA125 values needing low loop diuretic doses. In this randomized study (1:1) the investigators seek to evaluate whether a CA125 loop diuretic guided management therapy is superior to a standard strategy. The primary endpoint is the magnitude of changes of renal function at 24 and 72 hours after initiation of intravenous diuretic in an acute worsening of heart failure

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure
Keywords
Heart Failure, Renal Failure, Biomarker guided-therapy, Loop diuretics, Carbohydrate antigen 125

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
170 (Actual)

8. Arms, Groups, and Interventions

Arm Title
CA125 guided strategy
Arm Type
Experimental
Arm Description
In this group loop diuretic (Furosemide) dosage will be guided by Carbohydrate Antigen 125 (CA125) plasma levels
Arm Title
Conventional strategy
Arm Type
Active Comparator
Arm Description
Standard treatment strategy Therapy is based on established european guidelines
Intervention Type
Drug
Intervention Name(s)
CA125 guided strategy
Other Intervention Name(s)
Loop diuretic (Furosemide) dosage in CA125 ≤35 U/ml patients
Intervention Description
Initial dose of intravenous furosemide ≤80 mg / day regardless of prior dose of loop diuretics who were receiving.
Intervention Type
Drug
Intervention Name(s)
CA125 guided strategy
Other Intervention Name(s)
Loop diuretic dosage (Furosemide) in CA125 >35 U/ml patients
Intervention Description
Initial dose of intravenous furosemide ≥120 mg/day or 2.5 times the dose the patient was taking at home.
Intervention Type
Drug
Intervention Name(s)
Conventional Strategy
Intervention Description
The dosage of loop diuretics is done according to the presence of symptoms and signs of systemic congestion and current recommendations
Primary Outcome Measure Information:
Title
Change in renal function (GFR)
Description
Glomerular filtration rate (GFR) estimated by MDRD. Prespecified interim analysis of primary outcome will be made by protocol when first 100 patients are included.
Time Frame
24 and 72 hours
Secondary Outcome Measure Information:
Title
Improvement in signs and symptoms of heart failure (NYHA)
Description
Evaluation of dyspnea (changes in the functional class of the New York Heart Association -NYHA)
Time Frame
24 and 72 hours
Title
Improvement in signs and symptoms of heart failure (VAS)
Description
Evaluation of signs of systemic congestion, and patient global assessment (by visual analogue scale -VAS-)
Time Frame
24 and 72 hours
Title
Changes in plasma levels of natriuretic peptide (NT-proBNP)
Time Frame
72 hours
Title
Changes in plasma levels of high sensitive troponin
Time Frame
72 hours
Title
Time required to change intravenous diuretics to oral administration.
Time Frame
Through study completion (30-day follow-up)
Title
Composite of all-cause mortality plus acute heart failure related rehospitalization
Description
Number of events in each group during 30-day follow-up
Time Frame
30 days
Title
Change in renal function (creatinin)
Description
Serum levels of creatinine
Time Frame
24 h, 72 h and 30 days
Title
Change in renal function (urea)
Description
Serum levels of urea
Time Frame
24 h, 72 h and 30 days
Title
Change in renal function (cystatin C)
Description
Serum levels of Cystatin C
Time Frame
24 h, 72 h and 30 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with the diagnosis of acute heart failure (AHF) and the concurrence of the following conditions: Presence of symptoms (dyspnea at rest or minimal exertion) and signs attributable to congestion (signs of congestion on chest radiography, or presence of peripheral edema or ascites, or jugular venous distension at 45 degrees or presence of crackles on auscultation). Elevated natriuretic peptide (NT-proBNP> 1000 pg/ml or BNP> 100 mg/dl). Creatinine ≥1,4 mg/dl on admission, provided that the estimated glomerular filtration rate less than 60 ml / min / m2. Intent to be treated with loop diuretics intravenously. Exclusion Criteria: Life expectancy less than 6 months of life due to other comorbid conditions. Cardiogenic shock. Diagnosis of acute coronary syndrome in the previous 30 days. Pregnancy at the time of inclusion. Restrictive or Obstructive pulmonary disease or severe degree. Chronic renal insufficiency in stage V (estimated glomerular filtration rate <15 ml / min / m2) or patient previously included in known dialysis program. Participation in another clinical trial randomized at the time of inclusion. Temperature ≥38 ° C or diagnosis of pneumonia.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Julio Nuñez, MD, PhD
Organizational Affiliation
Fundación para la Investigación del Hospital Clínico de Valencia
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Clínico Universitario de Valencia
City
Valencia
ZIP/Postal Code
46010
Country
Spain

12. IPD Sharing Statement

Citations:
PubMed Identifier
32624444
Citation
de la Espriella R, Nunez E, Llacer P, Garcia-Blas S, Ventura S, Nunez JM, Sanchez R, Facila L, Vaquer JM, Bodi V, Santas E, Minana G, Mollar A, Nunez G, Chorro FJ, Gorriz JL, Sanchis J, Bayes-Genis A, Nunez J. Early urinary sodium trajectory and risk of adverse outcomes in acute heart failure and renal dysfunction. Rev Esp Cardiol (Engl Ed). 2021 Jul;74(7):616-623. doi: 10.1016/j.rec.2020.06.004. Epub 2020 Jul 2. English, Spanish.
Results Reference
derived

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Loop Diuretic Dosage in Patients With Acute Heart Failure and Renal Failure: Conventional Versus Carbohydrate Antigen 125-guided Therapy (IMPROVE-HF)

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