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The Role of Adrenomedullin on the Outcome of Severe Heart Failure: a Clinical Randomized Study

Primary Purpose

Heart Failure

Status
Withdrawn
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
clinical treatment
ultrafiltration
isovolumetric hemofiltration
Sponsored by
Federal University of São Paulo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Heart Failure focused on measuring adrenomedullin, heart failure, ultrafiltration, hemofiltration

Eligibility Criteria

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

Inclusion Criteria:

  • more than two item:

    • more than eighteen years of age
    • orthopnea
    • Chest Rx with cardiomegaly and pulmonary infiltration
    • edema
    • diuretic resistance

Exclusion Criteria:

  • insulin dependent diabetes
  • hepatic cirrhosis
  • vascular access problems
  • creatinine more than 2,5 mg/dl before acute heart failure
  • systemic infection
  • aortic stenosis and heart transplantation
  • radiologic contrast up to 72 hours prior randomization
  • advanced neoplasia

Sites / Locations

  • Instituto de Cardiologia

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Other

Experimental

Experimental

Arm Label

clinical treatment

ultrafiltration

isovolumetric hemofiltration

Arm Description

Patients with previous diagnosis of decompensated III and IV Heart Failure will be included. The clinical treatment will be optimized. Clinical assessment, Adrenomedullin, Angiotensin II, Brain Natriuretic Peptide, oxydative stress, sympathetic nervous system activity will be evaluated at the beginning, at discharge and 90 days after randomization(plus or minus3).

ultrafiltration will be done on decompensated patients III and IV acute heart failure on Intensive Care Unit. This patients will have biochemical analysis, adrenomedullin, angiotensin II,Brain Natriuretic Peptide, oxydative stress measurements,sympathetic nervous system activity evaluated and clinical outcome analyzed at the beginning,at discharge and 90 days after randomization(plus or minus 3). Diuretic will be withdrawn during ultrafiltration.

Patients randomized to this group will have isovolumetric hemofiltration on Intensive Care Unit. They will have biochemical analysis, Adrenomedullin plasmatic level, Brain Natriuretic Peptide Level, Angiotensin II level, Oxydative stress measurement,sympathetic nervous system, and clinical outcome evaluated at the study beginning,at discharge and 90 days after randomization(plus or minus 3).

Outcomes

Primary Outcome Measures

Levels of Adrenomedullin plasma in different treatments- clinical,ultrafiltration and isovolumetric hemofiltration
The adrenomedullin level will be compared in three different treatments: clinical treatment, ultrafiltration treatment and isovolumetric hemofiltration.
Levels of Adrenomedullin plasma in different treatments- clinical,ultrafiltration and isovolumetric hemofiltration
The adrenomedullin level will be compared in three different treatments: clinical treatment, ultrafiltration treatment and isovolumetric hemofiltration. The patients will be followed until discharge.

Secondary Outcome Measures

The Adrenomedullin plasma levels in three different treatment approaches will be related to clinical outcome.
The correlation of adrenomedullin plasma levels in all 3 arms related to optimized clinical outcome. The patients will be followed until discharge
The Adrenomedullin plasma levels in three different treatment approaches will be related to clinical outcome.
The correlation of adrenomedullin plasma levels in all 3 arms related to optimized clinical outcome.
The Adrenomedullin plasma levels in three different treatment approaches will be related to oxydative stress
The correlation of adrenomedullin plasma levels in all 3 arms related to oxydative stress. The patients will be followed until discharge.
The Adrenomedullin plasma levels in three different treatment approaches will be related to oxydative stress
The correlation of adrenomedullin plasma levels in all 3 arms related to oxydative stress.
The Adrenomedullin plasma levels in three different treatment approaches will be related to angiotensin II plasma level
The correlation of adrenomedullin plasma levels in all 3 arms related to angiotensin II level. The patients will be followed until discharge.
The Adrenomedullin plasma levels in three different treatment approaches will be related to angiotensin II plasma level
The correlation of adrenomedullin plasma levels in all 3 arms related to angiotensin II plasma level.
The Adrenomedullin plasma levels in three different treatment approaches will be related to Brain natriuretic peptide plasma level
The correlation of adrenomedullin plasma levels in all 3 arms related to Brain natriuretic peptide level. The patients will be followed until discharge.
The Adrenomedullin plasma levels in three different treatment approaches will be related to Pro-Brain natriuretic peptide plasma level
The correlation of adrenomedullin plasma levels in all 3 arms related to Brain natriuretic peptide level, 90 days after randomization(plus or minus 3)
The Adrenomedullin plasma levels in three different treatment approaches will be related to sympathetic nervous system activity
The correlation of adrenomedullin plasma levels in all 3 arms related to sympathetic nervous system.The patients will be followed until discharge.
The Adrenomedullin plasma levels in three different treatment approaches will be related to sympathetic nervous system activity
The correlation of adrenomedullin plasma levels in all 3 arms related to sympathetic nervous system.

Full Information

First Posted
June 28, 2010
Last Updated
November 2, 2016
Sponsor
Federal University of São Paulo
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1. Study Identification

Unique Protocol Identification Number
NCT01154504
Brief Title
The Role of Adrenomedullin on the Outcome of Severe Heart Failure: a Clinical Randomized Study
Official Title
The Role of Adrenomedullin on the Outcome of Severe Heart Failure: a Clinical Randomized Study
Study Type
Interventional

2. Study Status

Record Verification Date
November 2016
Overall Recruitment Status
Withdrawn
Why Stopped
We randomized 18 patients, but was impossible to measure adrenomedullin in Brazil. However, we analysed some interesting clinical and laboratorial results.
Study Start Date
April 2010 (undefined)
Primary Completion Date
December 2010 (Actual)
Study Completion Date
December 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Federal University of São Paulo

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Study Hypothesis: The decrease of plasma adrenomedullin (ADM) concentration by ultrafiltration and isovolumetric hemofiltration in patients with acute III and IV Class New York Heart Association Functional(NYHA) heart failure is more pronounced than a standard diuretic treatment and is related with clinical improvement. Outcome Measurements: To correlate the adrenomedullin plasma levels with clinical treatment, ultrafiltration and hemofiltration related to: Brain natriuretic peptide (BNP) level angiotensin II level sympathetic nervous activity oxydative stress clinical outcome at the beginning, at discharge and 90 days after randomization.
Detailed Description
Testing the hypothesis that adrenomedullin (ADM) is a important peptide in severe heart failure and that is related to clinical condition, we will study the effects of 3 different treatments (clinical usual treatment,ultrafiltration and isovolumetric hemofiltration with diuretics) to participants are followed until discharge to Adrenomedullin level and clinical outcomes,and also their relationship with angiotensin II level, brain natriuretic peptide(BNP), sympathetic nervous system and oxydative stress. The patients will be randomized in three different treatment group and analyzed in three moments: on the randomization, at discharge and 90 days after randomization(plus or minus 3). The clinical treatment will be optimized, the ultrafiltration will be done until clinically adequate fluid removal or until hematocrit increased 10% from basal level, and isovolumetric hemofiltration will be done for 8 hours- dose of 35 ml/kg/h in association with diuretic. All this dialytic procedures will be done with PAES membrane- filter HF1400 and automatic machine.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure
Keywords
adrenomedullin, heart failure, ultrafiltration, hemofiltration

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
clinical treatment
Arm Type
Other
Arm Description
Patients with previous diagnosis of decompensated III and IV Heart Failure will be included. The clinical treatment will be optimized. Clinical assessment, Adrenomedullin, Angiotensin II, Brain Natriuretic Peptide, oxydative stress, sympathetic nervous system activity will be evaluated at the beginning, at discharge and 90 days after randomization(plus or minus3).
Arm Title
ultrafiltration
Arm Type
Experimental
Arm Description
ultrafiltration will be done on decompensated patients III and IV acute heart failure on Intensive Care Unit. This patients will have biochemical analysis, adrenomedullin, angiotensin II,Brain Natriuretic Peptide, oxydative stress measurements,sympathetic nervous system activity evaluated and clinical outcome analyzed at the beginning,at discharge and 90 days after randomization(plus or minus 3). Diuretic will be withdrawn during ultrafiltration.
Arm Title
isovolumetric hemofiltration
Arm Type
Experimental
Arm Description
Patients randomized to this group will have isovolumetric hemofiltration on Intensive Care Unit. They will have biochemical analysis, Adrenomedullin plasmatic level, Brain Natriuretic Peptide Level, Angiotensin II level, Oxydative stress measurement,sympathetic nervous system, and clinical outcome evaluated at the study beginning,at discharge and 90 days after randomization(plus or minus 3).
Intervention Type
Other
Intervention Name(s)
clinical treatment
Other Intervention Name(s)
adrenomedullin
Intervention Description
The clinical treatment will be optimized to gold standard international heart failure treatment
Intervention Type
Procedure
Intervention Name(s)
ultrafiltration
Other Intervention Name(s)
dialysis, adrenomedullin
Intervention Description
The ultrafiltration procedure will be done on Intensive Care Unit with automatic machine and HF 1400 filter. The fluid will be removed until a increased of 10% in hematocrit or clinical improvement.
Intervention Type
Procedure
Intervention Name(s)
isovolumetric hemofiltration
Other Intervention Name(s)
hemofiltration, dialysis, adrenomedullin
Intervention Description
The isovolumetric hemofiltration will be done in Intensive Care Unit for 8 hours, and will be permitted the diuretic use.The dose will be 35 ml/kg/hour and will e used automatic machine and MF1400 filter.Diuretic use will be maintained.
Primary Outcome Measure Information:
Title
Levels of Adrenomedullin plasma in different treatments- clinical,ultrafiltration and isovolumetric hemofiltration
Description
The adrenomedullin level will be compared in three different treatments: clinical treatment, ultrafiltration treatment and isovolumetric hemofiltration.
Time Frame
90 days after randomization (plus or minus 3 days).
Title
Levels of Adrenomedullin plasma in different treatments- clinical,ultrafiltration and isovolumetric hemofiltration
Description
The adrenomedullin level will be compared in three different treatments: clinical treatment, ultrafiltration treatment and isovolumetric hemofiltration. The patients will be followed until discharge.
Time Frame
at discharge
Secondary Outcome Measure Information:
Title
The Adrenomedullin plasma levels in three different treatment approaches will be related to clinical outcome.
Description
The correlation of adrenomedullin plasma levels in all 3 arms related to optimized clinical outcome. The patients will be followed until discharge
Time Frame
at discharge
Title
The Adrenomedullin plasma levels in three different treatment approaches will be related to clinical outcome.
Description
The correlation of adrenomedullin plasma levels in all 3 arms related to optimized clinical outcome.
Time Frame
90 days after randomization (plus or minus 3)
Title
The Adrenomedullin plasma levels in three different treatment approaches will be related to oxydative stress
Description
The correlation of adrenomedullin plasma levels in all 3 arms related to oxydative stress. The patients will be followed until discharge.
Time Frame
at discharge
Title
The Adrenomedullin plasma levels in three different treatment approaches will be related to oxydative stress
Description
The correlation of adrenomedullin plasma levels in all 3 arms related to oxydative stress.
Time Frame
90 days after randomization(plus or minus 3)
Title
The Adrenomedullin plasma levels in three different treatment approaches will be related to angiotensin II plasma level
Description
The correlation of adrenomedullin plasma levels in all 3 arms related to angiotensin II level. The patients will be followed until discharge.
Time Frame
at discharge
Title
The Adrenomedullin plasma levels in three different treatment approaches will be related to angiotensin II plasma level
Description
The correlation of adrenomedullin plasma levels in all 3 arms related to angiotensin II plasma level.
Time Frame
90 days after randomization(plus or minus 3)
Title
The Adrenomedullin plasma levels in three different treatment approaches will be related to Brain natriuretic peptide plasma level
Description
The correlation of adrenomedullin plasma levels in all 3 arms related to Brain natriuretic peptide level. The patients will be followed until discharge.
Time Frame
at discharge
Title
The Adrenomedullin plasma levels in three different treatment approaches will be related to Pro-Brain natriuretic peptide plasma level
Description
The correlation of adrenomedullin plasma levels in all 3 arms related to Brain natriuretic peptide level, 90 days after randomization(plus or minus 3)
Time Frame
90 days after randomization(plus or minus 3)
Title
The Adrenomedullin plasma levels in three different treatment approaches will be related to sympathetic nervous system activity
Description
The correlation of adrenomedullin plasma levels in all 3 arms related to sympathetic nervous system.The patients will be followed until discharge.
Time Frame
at discharge
Title
The Adrenomedullin plasma levels in three different treatment approaches will be related to sympathetic nervous system activity
Description
The correlation of adrenomedullin plasma levels in all 3 arms related to sympathetic nervous system.
Time Frame
90 days after randomization(plus or minus 3)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: more than two item: more than eighteen years of age orthopnea Chest Rx with cardiomegaly and pulmonary infiltration edema diuretic resistance Exclusion Criteria: insulin dependent diabetes hepatic cirrhosis vascular access problems creatinine more than 2,5 mg/dl before acute heart failure systemic infection aortic stenosis and heart transplantation radiologic contrast up to 72 hours prior randomization advanced neoplasia
Facility Information:
Facility Name
Instituto de Cardiologia
City
Porto Alegre
State/Province
Rio Grande do Sul
ZIP/Postal Code
94801970
Country
Brazil

12. IPD Sharing Statement

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The Role of Adrenomedullin on the Outcome of Severe Heart Failure: a Clinical Randomized Study

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