Current partner codePEPTIDESDE
NCT04553484·Not applicable·OBSERVATIONAL

Measuring Cardiovascular Performance and Blood Flow Using Common But Never Compared Methods.

Status

Completed

Phase

Not applicable

Enrollment

657

Locations

4

Results

Posted

Publications

0

Study summary

What the protocol is testing.

Measuring Cardiovascular Performance Using Common Methods in subjects.

Full detailed description

This study will conduct measurements of cardiovascular performance by echocardiography (Echo), Brain Natriuretic Peptide (BNP) blood serum levels and blood flow by volume plethysmography (VP) in subjects who meet the AHA/ACC criteria for screening for peripheral arterial disease (PAD).

Interventions

Treatment arms and agents.

DIAGNOSTIC_TEST

No intervention

No intervention

Timeline

From registration to results.

  1. First posted

    Sep 17, 2020

  2. Study start

    Aug 5, 2020

  3. Primary completion

    Dec 29, 2021

  4. Study completion

    Jan 14, 2022

  5. Results posted

    Jul 3, 2024

  6. Registry updated

    Jul 3, 2024

Outcomes

What the study measures.

Primary outcomes

Feasibility of Performing Echo, BNP, and VP on Human Subjects.

Time frame · Baseline

The feasibility of performing three common tests, Echocardiography (Echo), Brain Natriuretic Peptide (BNP) and volume plethysmography (VP), in the same subject was assessed. Each of the 657 participants were submitted to a brief non-invasive blood flow and cardiac performance test (plethysmography (VP) and Echocardiography (Echo)). Each of the 236 participants were subject to blood drawn test, Brain Natriuretic Peptide (BNP).

Secondary outcomes

Not reported in the indexed record.

Eligibility

Who can take part.

Minimum age
45 Years
Maximum age
Not reported
Sex
ALL
Healthy volunteers
No

Inclusion Criteria: * At least 50 Patients from New York Heart Association (NYHA) Class 1 (One or more AHA Risk Factors, asymptomatic), ≤75% (36) Male, ≥25% (12) Female * At least 50 Patients from NYHA Class 2 (symptomatic), ≤75% (36) Male, ≥25% (12) Female Exclusion Criteria: * Subjects on mechanical ventilation. * Subjects who require decisions by a medical power of attorney. * Subjects unable to safely perform forced expiration. * Subjects with known technically difficult (TDS) trans-thoracic echocardiographic windows.

Study locations

4 registered sites.

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

Middle Georgia Heart and Vascular Center

Macon, Georgia, United States

Integrated Cardiology Group, LLC, d/b/a Bryan Heart

Lincoln, Nebraska, United States

JF Southwest Heart Clinic, P.A.

Houston, Texas, United States

Southwest Clinical Trials

Houston, Texas, United States

Publications

Results and literature.

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

Primary links

Continue at the source.

Related trials

More studies on Nesiritide.

Related PeptideStat pages

Put the record in context.

Research pages describe evidence. Vendor pages, where available, describe independently tracked research-product listings and are not clinical recommendations.