We updated the design of this site on December 18, 2017. Learn more.
ClinicalTrials.gov
ClinicalTrials.gov Menu

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

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.
ClinicalTrials.gov Identifier: NCT01292759
Recruitment Status : Unknown
Verified July 2010 by Johannes Gutenberg University Mainz.
Recruitment status was:  Recruiting
First Posted : February 10, 2011
Last Update Posted : February 15, 2011
Sponsor:
Information provided by:
Johannes Gutenberg University Mainz

Brief Summary:
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 or disease
Surgical Procedure, Unspecified

Study Type : Observational
Estimated Enrollment : 24 participants
Observational Model: Case-Only
Time Perspective: Prospective
Official Title: An Evaluation of a New, Non-invasive Monitoring Device in Major Abdominal Surgery Patients
Study Start Date : July 2010




Information from the National Library of Medicine

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, Learn About Clinical Studies.


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

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

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

Keywords provided by Johannes Gutenberg University Mainz:
stroke volume
cardiac output
validation