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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02296593
Other study ID # A14-D36-VOL.22
Secondary ID
Status Completed
Phase N/A
First received November 18, 2014
Last updated March 6, 2017
Start date November 2014
Est. completion date November 2016

Study information

Verified date March 2017
Source University Hospital, Caen
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Continuous lactate and glucose blood levels


Description:

MAQUET Group offers a new device that gives real time blood lactate and glucose levels. It is a new central veinous catheter with a microdialysis system. It is planted in the superior vena cava. It has not yet been used and validated with a clinical purpose, and particularly in cardiac surgery.

For now, reference method for determining blood lactate and glucose levels is co oxymetry.

This new simple device could provide great fluency for determining blood lactate and glucose levels. It could allow medical teams gain time for diagnosis and treatment of both hyperlactatemia and hyperglycemia.

The primary outcome of this study was to compare blood lactate and glucose absolute measures provided with the MAQUET new device (Maquet Critical Care AB, Solna, Sweden) and with co oxymetry.

The secondary outcome of this study was to compare variations of these absolutes measures.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date November 2016
Est. primary completion date May 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Men or women more than 18 years old.

- Cardiac surgery.

- Central veinous catheter in superior vena cava.

Exclusion Criteria:

- Men or women less than 18 years old.

- Pregnant women.

- Central veinous catheter not in superior vena cava.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
comparison of blood lactate and glucose levels
comparison of blood lactate and glucose levels with the reference method (co oxymetry) and a new central veinous catheter microdialysis system provided by MAQUET. (Critical Care AB, Solna, Sweden.)

Locations

Country Name City State
France CHU de Caen Caen Basse Normandie

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Caen

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary comparison of absolute blood lactate and glucose levels with the reference method (co oxymetry) and a new method using a device providing real time measures of lactate and glycemia with a central veinous catheter microdialysis system. Central veinous catheter, EIRUS (Maquet Critical Care AB, Solna, Sweden) 1 day
Secondary comparison of variations of blood lactate and glycemia levels with the reference method (co oxymetry) and a new method using a device providing real time measures of lactate and glycemia. (EIRUS) with a central veinous catheter microdialysis system. Central veinous catheter, EIRUS (Maquet Critical Care AB, Solna, Sweden) 1 day
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