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A study to determine whether in patients undergoing cardiac surgery, preoperative anxiety results in greater post-operative pain

Evaluation of postoperative pain after cardiothoracic surgery in patients with and without significant preoperative anxiety: A prospective observational study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2021/11/037728
Enrollment
122
Registered
2021-11-01
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: I251- Atherosclerotic heart disease of native coronary artery Health Condition 2: I083- Combined rheumatic disorders of mitral, aortic and tricuspid valves Health Condition 3: I38- Endocarditis, valve unspecified Health Condition 4: I712- Thoracic aortic aneurysm, withoutrupture

Interventions

None listed

Sponsors

JIPMER
Lead Sponsor

Eligibility

Inclusion criteria

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

Exclusion criteria: Patients requiring preoperative inotropes, mechanical ventilation, and intraââ?¬?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

Design outcomes

Primary

MeasureTime frame
IV Fentanyl consumptionTimepoint: 24 hours—

Secondary

MeasureTime frame
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—

Countries

India

Contacts

Public ContactDR SATYEN PARIDA

JIPMER, Puducherry

jipmersatyen@gmail.com9940973502

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026