Cardiac Output Monitoring in Aortic Aneurysm Surgery

Aneurysm Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01094938
• Other study ID #: EDICOAAS
• Secondary ID: 07/S1102/30
• Status: Completed
• Phase: N/A
• First received: March 26, 2010
• Last updated: March 26, 2010
• Start date: July 2007
• Est. completion date: July 2008

Study information

• Verified date: March 2010
• Source: NHS Lothian
• Contact: n/a
• Is FDA regulated: No
• Health authority: United Kingdom: Research Ethics Committee
• Study type: Observational

Clinical Trial Summary

To compare CO values obtained by the lithium indicator dilution method and pulse power analysis before, during and after anaesthesia and surgery for the elective repair of abdominal aortic aneurysms. This will enable us to determine how often and when calibration of the pulse power analysis derived CO is required.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 30
• Est. completion date: July 2008
• Est. primary completion date: July 2007
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patients presenting for elective abdominal aortic and extent 4 thoracoabdominal aortic aneurysm repair

Exclusion Criteria:

• Patients not giving informed consent.

• Patients under the age of 18 years.

• Patients who may be pregnant

• Patients with learning disabilities.

• Rhythm other than sinus rhythm.

• Patients on oral lithium therapy.

• Patients less than 40kg

• Patients with severe mitral regurgitation

Study Design

N/A

Related Conditions & MeSH terms

• Aneurysm
• Aortic Aneurysm

Locations

Country	Name	City	State
United Kingdom	NHS Lothian	Edinburgh

Sponsors (1)

Lead Sponsor	Collaborator
NHS Lothian

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Cardiac output
Secondary	Arterial Pressure