RECOGNISE: Using a Cerebral Oximeter monitoring device to identify and reduce postoperative complications in cardiac surgery

Not Applicable

• Conditions: Perioperative Medicine; Surgery; Anaesthesia, Perioperative Medicine and Pain Management

• Registration Number: ISRCTN12937489
• Lead Sponsor: niversity Hospital Of South Manchester NHS Foundation Trust

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2018-01-09
• Last Update Posted: 27 April 2020
• Study Completion: 2020-06-30

Recruitment & Eligibility

• Status: Ongoing
• Sex: All
• Target Recruitment: 440

Inclusion Criteria

1. Participant is willing and able to give informed consent for participation in the study
2. Male or Female, aged 18 years or above at point of consent
3. Participant is due to undergo elective or urgent cardiac surgery
4. Able (in the Investigators opinion) and willing to comply with all study requirements

Exclusion Criteria

1. Patients undergoing emergency cardiac surgery
2. Participant undergoing transplantation surgery or Mechanical Circulatory Support Implantation surgery.
3. Participants undergoing aortic surgery with Deep Hypothermic Circulatory Arrest
4. Patients already unconscious, sedated or anaesthetised before surgery
5. Patients unable to provide informed consent
6. Significant alcohol intake preoperatively (> 50 units/week)
7. Any other significant disease or disorder which, in the opinion of the Investigator, may either put the participants at risk because of participation in the study, or may influence the result of the study, or the participant’s ability to participate in the study

Study & Design

• Study Type: Interventional
• Study Design: Not specified