ClinicalTrials.Veeva

Menu

Cardiac Output Monitoring in Aortic Aneurysm Surgery

N

NHS Lothian

Status

Completed

Conditions

Aneurysm

Study type

Observational

Funder types

Other

Identifiers

NCT01094938
EDICOAAS
07/S1102/30 (Other Identifier)

Details and patient eligibility

About

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.

Enrollment

30 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

30 participants in 1 patient group

Repair

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems