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

The recruitment status of this study is unknown because the information has not been verified recently.

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

Sponsor:

Information provided by:

Johannes Gutenberg University Mainz

ClinicalTrials.gov Identifier:

NCT01292759

First received: February 9, 2011

Last updated: February 14, 2011

Last verified: July 2010

History of Changes

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


Ages Eligible for Study:	18 Years to 80 Years
Genders Eligible for Study:	Both
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

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: 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

No publications provided


Responsible Party:	Larissa Philippi, Klinik für Anästhesie
ClinicalTrials.gov Identifier:	NCT01292759 History of Changes
Other Study ID Numbers:	837.194.10 (7203)
Study First Received:	February 9, 2011
Last Updated:	February 14, 2011
Health Authority:	Germany: Ethics Commission

Keywords provided by Johannes Gutenberg University Mainz:


stroke volume cardiac output validation

ClinicalTrials.gov processed this record on March 03, 2015

To Top