To measure the adequacy of anaesthesia.
Not Applicable
Completed
- Conditions
- Health Condition 1: null- PATENTS POSTED FOR CARDIOPULMONARY BYPASS SURGERY
- Registration Number
- CTRI/2017/10/010134
- Lead Sponsor
- Pragya Sachan
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 100
Inclusion Criteria
Patients aged 18-60 years and consenting for monitoring were included in study
Exclusion Criteria
Patients unwilling and with history of epilepsy,head injury,thromboembolic episodes related or unrelated to cardiac disease were excluded from study.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method monitor the depth of <br/ ><br>Anaesthesia using Entropy monitor during <br/ ><br>Cardiopulmonary bypass on the basis of Numerical Indices provided by Entropy Monitor (Response Entropy {RE} and State Entropy {SE}, Burst Suppression Ratio{BSR} <br/ ><br>Timepoint: After 18 months of study.
- Secondary Outcome Measures
Name Time Method Modified Version of Brice Questionnaire used after 48 hrs of Surgery about any <br/ ><br>memories or recall of Intra operative awareness.Timepoint: AFTER 48 HOURS