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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
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 June 17, 2013