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TerminatedNCT03262571Updated Aug 25, 2017

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

A Phase 3 interventional study of Lung ultrasound in Chronic Heart Failure, Lung; Congestive and Acute Decompensated Heart Failure, sponsored by IRCCS San Raffaele. Terminated at 1 site in Italy. Open to participants aged 18 Years to 90 Years. Per ClinicalTrials.gov, last updated 2017-08-25.

Sponsored by IRCCS San Raffaele · Phase 3, Interventional, and Treatment

Why this study was terminated
Because at the interim analysis the pre-specified stopping boundary for an overwhelming benefit had been crossed.
Phase
Phase 3
Study type
Interventional
Enrollment
244
Allocation
Randomized
Ages
18 Years to 90 Years
Sex
All
01

Study 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.

02

Conditions studied

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

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Keywords

  • Heart failure
  • Lung ultrasound
  • B-lines
03

Who can participate

Ages eligible
18 Years to 90 Years
Sexes eligible
All
Accepts healthy volunteers
No

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

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.

04

Study design

Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
244 participants (actual)

Study arms

  • Experimental
    Group A

    Group A includes patients undergoing lung ultrasound and physical examination.

    Diagnostic Test: Lung ultrasound

  • Placebo comparator
    Group B

    Group B includes patients undergoing physical examination only.

    Diagnostic Test: Lung ultrasound

Interventions

  • Diagnostic testLung ultrasound

    Duretic therapy is then optimized according to the presence and severity of B-lines in group A.

05

What researchers measure

Primary outcomes

  1. 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.

    Time frame: 90 days

Secondary outcomes

  1. Natriuretic peptides values

    Significant reduction of natriuretic peptides values in group A during the 90-day follow-up period.

    Time frame: 90 days

  2. Quality of life test (QLT) score

    Significant reduction of QTL score in group A during the 90-day follow-up period.

    Time frame: 90 days

  3. Cardiac mortality

    Significant reduction of cardiac mortality rate in group A versus group B.

    Time frame: 90 days

06

Study locations

1 site
  • San Raffaele Hospital
    Milano, 20132, Italy
07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT03262571
Lead sponsor
IRCCS San Raffaele
Responsible party
Agricola Eustachio (MD, IRCCS San Raffaele) — Principal investigator
First posted
Aug 25, 2017
Start date
Dec 2010
Primary completion
Mar 2016
Completion
Mar 2016
Last update
Aug 25, 2017

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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