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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02335684
Other study ID # H-1-2013-103
Secondary ID
Status Completed
Phase N/A
First received January 20, 2014
Last updated October 26, 2015
Start date November 2013
Est. completion date October 2015

Study information

Verified date October 2015
Source Rigshospitalet, Denmark
Contact n/a
Is FDA regulated No
Health authority Denmark: Ethics Committee
Study type Interventional

Clinical Trial Summary

This randomized trial has been designed to study if it is possible to enhance work capacity during submaximal efforts in heart failure patients supported with continuous-flow left ventricular assist devices (CF-LVAD).

The hypothesis is that exercise tolerability during low to moderate workloads in CF-LVAD patients can be increased when pump speed is increased soon after the onset of exercise.


Description:

To test the hypothesis described above the investigators will study submaximal exercise tests below anaerobic threshold in patients supported with CF-LVADs.Each patient will perform two tests- one with baseline CF-LVAD pump speed and the other with incrementally increased pump speed.


Recruitment information / eligibility

Status Completed
Enrollment 31
Est. completion date October 2015
Est. primary completion date October 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Ischemic and non-ischemic cardiomyopathy patients with CF-LVADs,signed informed consent.

Exclusion Criteria:

- Unstable patients, CF-LVAD implantation less than three months ago.

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Investigator)


Related Conditions & MeSH terms


Intervention

Other:
CF-LVAD pump speed baseline.
Submaximal exercise test with baseline pump speed.
CF-LVAD pump speed increased.
Submaximal exercise test with increased pump speed (+800RPM).

Locations

Country Name City State
Denmark University Hospital of Copenhagen; Rigshospitalet. Copenhagen Oe

Sponsors (2)

Lead Sponsor Collaborator
Rigshospitalet, Denmark Danish Heart Foundation

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Other Heart rate Heart rate is measured by ECG monitoring. Heart rate will be measures during exercise. No
Other Anaerobic threshold Anaerobic threshold is defined as respiratory exchange rate (RER) >1. Anaerobic threshold is measured during exercise on the study day. No
Primary Exercise time Exercise will be performed on a upright ergometer bike with simultaneously breath-by-breath gaz analysis. Exercise time will be estimated only on the day of the study. No follow-up. No
Secondary Perceived exertion Rate of exertion will be estimated using the Borg Scale. Perceived exertion will be estimated during exercise on the ergometer bike on the day of the study. No
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