Current partner codePEPTIDESDE
NCT01734135·Not applicable·INTERVENTIONAL

Provider Notification for High B-type Natriuretic Peptide Values

Status

Completed

Phase

Not applicable

Enrollment

115

Locations

1

Results

Not posted

Publications

0

Study summary

What the protocol is testing.

This proposal examines use of a clinical reminder to the primary provider of patient with a high B type natriuretic peptide but no prior imaging. Electrical Medical Record-based Intervention to Determine whether Clinical Reminders Improve Heart Failure Management in Patients with High BNP Values and Unknown LVEF.

Full detailed description

Rationale: B type natriuretic peptide is known to be elevated (\> 100 pg/ml) in patients with heart failure. Furthermore, treatments are available to improve survival and reduce hospitalization if the left ventricular ejection fraction (LVEF) is \< 40%. Accordingly, guidelines recommend an LVEF measure for patients with suspected heart failure. Prior work has demonstrated that patients with high BNP values do not always have a measure of left ventricular ejection. Hypothesis: A reminder to patients with BNP and no imaging may prompt providers to order appropriate imaging potentially leading to 1) identification of unsuspected depressed ejection fraction and 2) more appropriate treatment.

Interventions

Treatment arms and agents.

OTHER

Clinical Reminder

A note is sent to the primary care provider using the electronic medical record indicating the high BNP result and potential benefit of measurement of the left ventricular ejection fraction. A draft order is placed for an echocardiogram for the provider to accept or delete.

Timeline

From registration to results.

  1. First posted

    Nov 27, 2012

  2. Study start

    Oct 2010

  3. Primary completion

    Sep 2013

  4. Study completion

    Sep 2015

  5. Results posted

    Not reported

  6. Registry updated

    Sep 19, 2025

Outcomes

What the study measures.

Primary outcomes

Measurement of left ventricular ejection fraction

Time frame · 6 months after randomization

numerator: Measurement of left ventricular ejection fraction within 6 months of randomization. denominator: All randomized patients

Secondary outcomes

Identification of LVEF < 40%

Time frame · 6 months following randomizaiton

Numerator: number of patients identified with an LVEF\< 40% Denominator: all randomized patients

Treatment of Low LVEF

Time frame · 6 months following randomization

Numerator: number of patients with an LVEF \< 40% and treatment with either an angiotensin converting enzyme inhibitor, angiotensin receptor blocker or evidence based beta-blocker (carvedilol, metoprolol succinate, bisoprolol). Denominator: all randomized patients.

Eligibility

Who can take part.

Minimum age
18 Years
Maximum age
120 Years
Sex
ALL
Healthy volunteers
No

Inclusion Criteria: * BNP \>= 200 pg/ml in last 2 months Exclusion Criteria: * Measure of LVEF in the last 12 months * Last measure of LVEF \< 40%

Study locations

1 registered sites.

United States. Showing up to 24 locations stored in the fast local snapshot.

VA Palo Alto Health Care System

Palo Alto, California, United States

Publications

Results and literature.

No PMID-linked publications were present in this registry snapshot.

Primary links

Continue at the source.

Related trials

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Related PeptideStat pages

Put the record in context.

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