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Usefulness of Lung Ultrasound in Ambulatory Management of Patients With Chronic Heart Failure

Primary Purpose

Chronic Heart Failure, Lung; Congestive, Acute Decompensated Heart Failure

Status
Terminated
Phase
Phase 3
Locations
Italy
Study Type
Interventional
Intervention
Lung ultrasound
Sponsored by
IRCCS San Raffaele
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Heart Failure focused on measuring Heart failure, Lung ultrasound, B-lines

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

(1) male and female aged between 18 and 90 years (2) signed written informed consent (3) history of HF for at least six months, (4) left ventricular ejection fraction < 45%, (5) adequate medical therapy for HF for at least two months.

Exclusion Criteria:

(1) concomitant enrollment in other clinical studies, or treatment with experimental drugs or devices within 30 days of clinical assessment, (2) inability to undergo to the planned follow-up and procedures (3) documented pulmonary infections (4) interstitial lung disease, class 4 chronic obstructive pulmonary disease according to GOLD guidelines (5) chronic dialysis.

Sites / Locations

  • San Raffaele Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Group A

Group B

Arm Description

Group A includes patients undergoing lung ultrasound and physical examination.

Group B includes patients undergoing physical examination only.

Outcomes

Primary Outcome Measures

Reduction of hospitalizations for acute decompensated heart failure
Significant reduction of hospitalizations for acute decompensated heart failure in group A during the 90-day follow-up period.

Secondary Outcome Measures

Natriuretic peptides values
Significant reduction of natriuretic peptides values in group A during the 90-day follow-up period.
Quality of life test (QLT) score
Significant reduction of QTL score in group A during the 90-day follow-up period.
Cardiac mortality
Significant reduction of cardiac mortality rate in group A versus group B.

Full Information

First Posted
August 23, 2017
Last Updated
August 24, 2017
Sponsor
IRCCS San Raffaele
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1. Study Identification

Unique Protocol Identification Number
NCT03262571
Brief Title
Usefulness of Lung Ultrasound in Ambulatory Management of Patients With Chronic Heart Failure
Official Title
Usefulness of Lung Ultrasound in Ambulatory Management of Patients With Chronic Heart Failure
Study Type
Interventional

2. Study Status

Record Verification Date
August 2017
Overall Recruitment Status
Terminated
Why Stopped
Because at the interim analysis the pre-specified stopping boundary for an overwhelming benefit had been crossed.
Study Start Date
December 2010 (Actual)
Primary Completion Date
March 2016 (Actual)
Study Completion Date
March 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
IRCCS San Raffaele

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Purpose. The aim of this study is to evaluate whether lung ultrasound, in addition to physical examination, leads to a reduction of the admission rate for acute decompensated heart failure of patients with chronic heart failure (HF) followed in the outpatients heart failure clinic. Methods. This is a prospective randomized study. The planned sample size consists of 440 patients with chronic HF. The inclusion criteria are: (1) male and female aged between 18 and 90 years (2) signed written informed consent (3) history of HF for at least six months, (4) left ventricular ejection fraction < 45%, (5) adequate medical therapy for HF for at least two months. The exclusion criteria are: (1) concomitant enrollment in other clinical studies, or treatment with experimental drugs or devices within 30 days of clinical assessment, (2) inability to undergo to the planned follow-up and procedures (3) documented pulmonary infections (3) interstitial lung disease and class 4 chronic obstructive pulmonary disease according to GOLD classification. Patients are randomized in two groups: group A, patients undergoing to lung ultrasound and physical examination; and group B, patients undergoing to physical examination only. Patients are evaluated at baseline and after three months with medical history, Quality of Life test, physical examination, blood sample for hematochemical (creatinine, electrolytes, BNP/NTpro-BNP). The diuretic therapy is then optimized according to the presence and severity of B-lines in group A and physical examination in group B. Only patients enrolled in group A undergo to a lung ultrasound examination to assess the extent of pulmonary congestion, through its evidence of B-lines. B-lines originate from the contrast between air-filled structures and water-thickened pulmonary interlobular septa. This leads to linear echogenic vertical artefacts that spread from the pleural layers downwards in the screen. The ultrasound examination is performed with a handheld echocardiography device. The physician carries out a scan of the pulmonary fields, from basal towards mid and apical fields, through the midaxillary line while the patient lies supine. The quantification of B-lines is performed according to their extent over the lung fields. All the information are recorded in dedicated forms. The results are evaluated according to the following criteria. The primary end-point is a significant reduction of hospitalizations for acute decompensated HF in group A during the follow-up period. The secondary end-points are changes of NT-proBNP values, quality of life test (QLT) score and cardiac mortality.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Heart Failure, Lung; Congestive, Acute Decompensated Heart Failure
Keywords
Heart failure, Lung ultrasound, B-lines

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
244 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Group A
Arm Type
Experimental
Arm Description
Group A includes patients undergoing lung ultrasound and physical examination.
Arm Title
Group B
Arm Type
Placebo Comparator
Arm Description
Group B includes patients undergoing physical examination only.
Intervention Type
Diagnostic Test
Intervention Name(s)
Lung ultrasound
Intervention Description
Duretic therapy is then optimized according to the presence and severity of B-lines in group A.
Primary Outcome Measure Information:
Title
Reduction of hospitalizations for acute decompensated heart failure
Description
Significant reduction of hospitalizations for acute decompensated heart failure in group A during the 90-day follow-up period.
Time Frame
90 days
Secondary Outcome Measure Information:
Title
Natriuretic peptides values
Description
Significant reduction of natriuretic peptides values in group A during the 90-day follow-up period.
Time Frame
90 days
Title
Quality of life test (QLT) score
Description
Significant reduction of QTL score in group A during the 90-day follow-up period.
Time Frame
90 days
Title
Cardiac mortality
Description
Significant reduction of cardiac mortality rate in group A versus group B.
Time Frame
90 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: (1) male and female aged between 18 and 90 years (2) signed written informed consent (3) history of HF for at least six months, (4) left ventricular ejection fraction < 45%, (5) adequate medical therapy for HF for at least two months. Exclusion Criteria: (1) concomitant enrollment in other clinical studies, or treatment with experimental drugs or devices within 30 days of clinical assessment, (2) inability to undergo to the planned follow-up and procedures (3) documented pulmonary infections (4) interstitial lung disease, class 4 chronic obstructive pulmonary disease according to GOLD guidelines (5) chronic dialysis.
Facility Information:
Facility Name
San Raffaele Hospital
City
Milano
ZIP/Postal Code
20132
Country
Italy

12. IPD Sharing Statement

Plan to Share IPD
No

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Usefulness of Lung Ultrasound in Ambulatory Management of Patients With Chronic Heart Failure

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