Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Intervention1: Nil: Nil
Intervention2: Nil: Nil
Sponsors
Sawai Mansingh Medical College and Hospital
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients giving informed written consent. 2. Aged between 18 to 65 years 3. Patients with ASA grade class II to III undergoing elective coronary artery bypass graft surgery. 4. Subjects capable of answering Amsterdam preoperative anxiety and information scale questionnaire.
Exclusion criteria
Exclusion criteria: 1. Patients who had undergone prior cardiothoracic procedure. 2. Participants giving history of opioid addiction. 3. Patients with other comorbidities. 4. Patients with any type of psychiatric illness or delirium before surgery. 5.Patients taking part in any other study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1) To assess and compare the postoperative visual analogue score in two groups 2) To determine the difference in the consumption of fentanyl post operatively between the two groups 3) To assess and compare the neuro cognitive function between the two groups Timepoint: 1) To assess the visual analogue score at 15 minutes and then 3,6,12, 18, 24, 30, 36, 42, 48 hours after extubation 2) To determine total dose of fentanyl within 48 hours after extubation. 3) To assess the neuro cognitive function by mini mental State examination on post op day 1, 2, 3 and 4. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1)To assess and compare the hemodynamic parameters between the two groups. 2)To determine the duration of ICU stay in days.Timepoint: To assess the hemodynamic parameters( mean arterial pressure , heart rate ) post operatively at 30 minute, 1 hour, 3, 6, 12, 18, 24, 30, 36, 42, 48 hours after extubation. | — |
Countries
India
Contacts
Public ContactDr Ranu Gandhi
Sawai Man Singh Medical College,Jaipur
Outcome results
None listed