Non-invasive Assessment of Arterial Blood Pressure and Functional Hemodynamic Parameters

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.

Verified July 2010 by Johannes Gutenberg University Mainz.
Recruitment status was: Recruiting

Sponsor:

ClinicalTrials.gov Identifier:

NCT01292759

First Posted: February 10, 2011

Last Update Posted: February 15, 2011

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.

Information provided by:

Johannes Gutenberg University Mainz

Purpose

Cardiac output can be monitored using different invasive devices. Nexfin HD is a new, noninvasive device that uses model flow technology to measure stroke volume and thus computes cardiac output (CO). To evaluate this new device the investigators compared esophageal doppler CO to Nexfin HD CO in patients scheduled for elective abdominal surgery.

Condition
Surgical Procedure, Unspecified


Study Type:	Observational
Study Design:	Observational Model: Case-Only Time Perspective: Prospective
Official Title:	An Evaluation of a New, Non-invasive Monitoring Device in Major Abdominal Surgery Patients

Further study details as provided by Johannes Gutenberg University Mainz:


Estimated Enrollment:	24
Study Start Date:	July 2010

Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:	18 Years to 80 Years (Adult, Senior)
Sexes Eligible for Study:	All
Accepts Healthy Volunteers:	No
Sampling Method:	Non-Probability Sample

Study Population

Patients scheduled for elective abdominal surgery

Criteria

Inclusion Criteria:

Age > 18 and < 80 years old
Written informed consent obtained

Exclusion Criteria:

Renal failure
Heart failure (EF < 25%)
Peripheral artery occlusion disease
M. Raynaud
Rhythms other than sinus

Contacts and Locations

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01292759

Locations


Germany
Klinik für Anaesthesiology der Universitätsmedizin Mainz	Recruiting
Mainz, Germany, 55131
Contact: Larissa Philippi l.philippi@web.de

Sponsors and Collaborators

Johannes Gutenberg University Mainz

More Information


Responsible Party:	Larissa Philippi, Klinik für Anästhesie
ClinicalTrials.gov Identifier:	NCT01292759 History of Changes
Other Study ID Numbers:	837.194.10 (7203)
First Submitted:	February 9, 2011
First Posted:	February 10, 2011
Last Update Posted:	February 15, 2011
Last Verified:	July 2010

Keywords provided by Johannes Gutenberg University Mainz:


stroke volume cardiac output validation

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