MedPath

Circadian disruption after anaesthesia and surgery in patients undergoing cardiac surgery.

Not Applicable
Completed
Conditions
Circadian disruption following cardiac surgery
Other - Research that is not of generic health relevance and not applicable to specific health categories listed above
Sleep disruption following cardiac surgery
Registration Number
ACTRN12608000640303
Lead Sponsor
niversity of Auckland
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
50
Inclusion Criteria

All patients presenting for elective bypass cardiac surgery

Exclusion Criteria

Refusal, non-bypass surgery, patient requiring Magnetic Resonance Imaging at any stage during treatment, congenital heart disease

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Sleep/ wake cycle disruption, the extent of which is measured using actigraphy and sleep diaries.[Three sets of measurements are taken - five to seven days pre-operatively, five to seven days immediately post-operatively and five to seven days immediately post-discharge. One sleep diary of one week is completed at each stage.];Circadian disruption, measured using vitalsense core body temperature monitoring equipment and salivary melatonin. Changes in melatonin levels and core body temperature show the extent, if any, of circadian disruption.[The three to four days of pre-operative core body temperature data, three to four days of post-operative data and three to four days of post-discharge data are collected. Salivary melatonin is also collected at nine half-hour intervals once at every stage. The pre-operative results are then compared to the post-operative to establish melatonin onset time and changes in core body temperature levels - these measurements are compared one week post-discharge.]
Secondary Outcome Measures
NameTimeMethod
Mood disturbance, measured using profile of mood states questionnaires[The profile of mood states questionnaire is taken one week pre-operatively, one week post-operatively and one week post-discharge. The results of the questionnaires are compared one week post-discharge.]
© Copyright 2025. All Rights Reserved by MedPath