A study to determine whether in patients undergoing cardiac surgery, preoperative anxiety results in greater post-operative pai
Not Applicable
Completed
- Conditions
- Health Condition 1: I251- Atherosclerotic heart disease of native coronary arteryHealth Condition 2: I083- Combined rheumatic disorders of mitral, aortic and tricuspid valvesHealth Condition 3: I38- Endocarditis, valve unspecifiedHealth Condition 4: I712- Thoracic aortic aneurysm, withoutrupture
- Registration Number
- CTRI/2021/11/037728
- Lead Sponsor
- JIPMER
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 122
Inclusion Criteria
Patients above the age of 18 years
Undergoing elective cardiothoracic surgery
Able to independently answer the Amsterdam Preoperative Anxiety and Information Scale (APAIS) questionnaire written in Tamil
Exclusion Criteria
Patients requiring preoperative inotropes, mechanical ventilation, and intra�aortic balloon counter pulsation
Previous cardiac surgery
Opioid addiction
Chronic liver disease
Chronic renal disease
Cognitive impairment
Incapable of providing written consent
Could not respond to investigatorsââ?¬• queries due to any reason
Patients proposed to be administered an alternative pain management option such as thoracic epidurals or some other form of regional anaesthesia
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method IV Fentanyl consumptionTimepoint: 24 hours
- Secondary Outcome Measures
Name Time Method Anxiety scoreTimepoint: Preoperatively;Factors associated with preoperative anxietyTimepoint: At analysis;Post-operative VASTimepoint: Eye opening, 12, 16, 20 and 24 hrs;Rescue analgesia with TramadolTimepoint: Over 24 hours