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Blood-pressure Measuring in Patients Carrying a Left Ventricular Assist Device (LVAD)

I

Insel Gruppe AG, University Hospital Bern

Status

Completed

Conditions

Left Ventricular Assist Device

Treatments

Device: Blood-pressure measuring (Nellcor™ Adult SpO2 Sensor)

Study type

Interventional

Funder types

Other

Identifiers

NCT03458988
2017-01570

Details and patient eligibility

About

To prove the novel device is able to reliably detect pulsatility in patients with CF-VADs and to analyze whether pre-programmed intrinsic pulsatility of the 3rd generation CF-VADs can also be picked up. The study is not designed to measure blood pressure.

Should this pilot study be successful in detecting enough pulsatility a follow-up study would then try to transfer the results into blood-pressure values with the help of comparators in order to identify an easier and more reliable method to measure BP in CF-VAD patients. .

Full description

The number of patients supported by left ventricular assist device (LVAD) is increasing as durable mechanical support has become widely available for end stage heart failure as destination therapy and as bridge to transplantation. The accurate measurement of blood pressure (BP) as well as the recognition and management of hypertension in patients with LVADs is an essential component of optimal clinical care. Hypertension is an established long-term risk factor for cardiovascular disease. The measurement of BP and the management of hypertension in patients with CF-VADs can present unique challenges. Patients with LVADs often do not have a palpable pulse, and therefore traditional BP measurement by auscultation or automated cuff is less reliable. Conventional occlusive BP measurement is able to to pick up signals in approximately 50% of cases due to coincidental phases of pulsatility. The arterial line is the gold standard, but is an invasive procedure and not practical for routine outpatient use.

Although efforts are underway to identify an easier and more reliable method to measure ambulatory BP in these patients not one has been able to match the quality of an invasive arterial line.

Enrollment

30 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients carrying one of the two third generation CF-VADS (Heartware HVAD, Heartmate 3)
  • Patients >18y
  • Good understanding of written and oral German
  • Signed informed consent
  • Scheduled for routine outpatient appointment.

Exclusion criteria

  • In the population of the outpatient clinic's CV-LVAD patients no known exclusion criteria exists

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

30 participants in 1 patient group

All patients
Other group
Description:
Nellcor™ Adult SpO2 Sensor
Treatment:
Device: Blood-pressure measuring (Nellcor™ Adult SpO2 Sensor)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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