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

Tracking Information
First Received Date ^ICMJE	February 9, 2011
Last Updated Date	February 14, 2011
Start Date ^ICMJE	July 2010
Primary Completion Date	Not Provided
Current Primary Outcome Measures ^ICMJE	Not Provided
Original Primary Outcome Measures ^ICMJE	Not Provided
Change History	Complete list of historical versions of study NCT01292759 on ClinicalTrials.gov Archive Site
Current Secondary Outcome Measures ^ICMJE	Not Provided
Original Secondary Outcome Measures ^ICMJE	Not Provided
Current Other Outcome Measures ^ICMJE	Not Provided
Original Other Outcome Measures ^ICMJE	Not Provided

Descriptive Information
Brief Title ^ICMJE	Non-invasive Assessment of Arterial Blood Pressure and Functional Hemodynamic Parameters
Official Title ^ICMJE	An Evaluation of a New, Non-invasive Monitoring Device in Major Abdominal Surgery Patients
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.
Detailed Description	Not Provided
Study Type ^ICMJE	Observational
Study Design ^ICMJE	Observational Model: Case-Only Time Perspective: Prospective
Target Follow-Up Duration	Not Provided
Biospecimen	Not Provided
Sampling Method	Non-Probability Sample
Study Population	Patients scheduled for elective abdominal surgery
Condition ^ICMJE	Surgical Procedure, Unspecified
Intervention ^ICMJE	Not Provided
Study Group/Cohort (s)	Not Provided
Publications *	Not Provided
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.

Recruitment Information
Recruitment Status ^ICMJE	Recruiting
Estimated Enrollment ^ICMJE	24
Completion Date	Not Provided
Primary Completion Date	Not Provided
Eligibility Criteria ^ICMJE	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
Gender	Both
Ages	18 Years to 80 Years
Accepts Healthy Volunteers	No
Contacts ^ICMJE	Not Provided
Location Countries ^ICMJE	Germany

Administrative Information
NCT Number ^ICMJE	NCT01292759
Other Study ID Numbers ^ICMJE	837.194.10 (7203)
Has Data Monitoring Committee	No
Responsible Party	Larissa Philippi, Klinik für Anästhesie
Study Sponsor ^ICMJE	Johannes Gutenberg University Mainz
Collaborators ^ICMJE	Not Provided
Investigators ^ICMJE	Not Provided
Information Provided By	Johannes Gutenberg University Mainz
Verification Date	July 2010
^ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP

To Top