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OpenTrials
Completed

NCT Number: NCT01094938

Cardiac Output Monitoring in Aortic Aneurysm Surgery

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.

Completed

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

NHS Lothian

Edinburgh, EH16 4SA, United Kingdom

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Primary outcomes

  1. Cardiac output

Secondary outcomes

  1. Arterial Pressure

Sponsors and collaborators

Lead sponsor

NHS Lothian

Other Gov

Registry information

Important dates

Study start
2007
Primary completion
2007
Study completion
2008
First posted
Mar 29, 2010
Registry last updated
Sep 23, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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