Clinical Trials Directory

Trials / Completed

CompletedNCT02481908

STI Combined to Valsalva Maneuver for the Diagnosis of Left Ventricular Dysfunction in COPD Exacerbations

a New and Non Invasive Method to Calculate STI ( Systolic Time Intervals) Combined to Valsalva Maneuver in Patient With Acute Exacerbation of COPD

Status
Completed
Phase
Study type
Observational
Enrollment
189 (actual)
Sponsor
University of Monastir · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The aim of this investigation was to assess the value of Systolic Time Intervals (STIs) as a method of detecting Left Ventricular Dysfunction (LVD) in patients admitted to the emergency department for cute exacerbations of chronic obstructive pulmonary disease (AECOPD) and whether STIs measured under Valsalva manoeuver (VM) could improve the distinction between patients with LVD and those without LVD.

Detailed description

We included patients admitted to the ED for AECOPD. Measurement of STIs included electromechanical activation time (EMAT), left ventricular ejection time and EMAT/LVET ratio. These were performed at baseline and during the first strain phase of the VM using a computerized phono and electrocardiographic method. The diagnosis of LVD was determined on the basis of clinical examination, echocardiography and brain natriuretic peptide. The values of STIs were compared between patients with and without LVD ; their diagnostic performance was assessed using the area under receiver operating characteristic curve (AUC of ROC).

Conditions

Interventions

TypeNameDescription
DEVICESTI measurements at baseline and under Valsalva maneuverSTI measurements at baseline and under Valsalva maneuver

Timeline

Start date
2012-04-01
Primary completion
2013-12-01
Completion
2013-12-01
First posted
2015-06-25
Last updated
2020-09-14

Locations

1 site across 1 country: Tunisia

Source: ClinicalTrials.gov record NCT02481908. Inclusion in this directory is not an endorsement.