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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
Recruitment status was: Recruiting
Sponsor:
Johannes Gutenberg University Mainz
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
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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:
Eligibility| 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
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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
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
| 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 |
Keywords provided by Johannes Gutenberg University Mainz:
|
stroke volume cardiac output validation |
ClinicalTrials.gov processed this record on August 23, 2017