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feasibility of anesthetic technique without opioid drugs in patients undergoing beating heart bypass operation

Feasibility of opioid free anesthesia in off pump coronary artery bypass surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/01/017046
Enrollment
30
Registered
2019-01-11
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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: I251- Atherosclerotic heart disease of native coronary artery Health Condition 3: I251- Atherosclerotic heart disease of native coronary artery

Interventions

Intervention1: Opioid based anesthetic technique: Opioid based anesthetic technique in patients undergoing off pump coronary artery bypass surgery Control Intervention1: Opioid free anesthetic techniq

Sponsors

Sri Jayadeva institute of Cardiovascular sciences and research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients scheduled for elective off-pump coronary artery bypass surgery

Exclusion criteria

Exclusion criteria: 1) patient refusal 2) allergy to local anesthetics 3) Localized infection 4) Coagulopathy/Bleeding diathesis/Patients on anticoagulants 5) Emergency conversion to On-pump surgery 6) spinal deformities 7) Left main coronary artery disease 8) Left Ventricular ejection fraction less than 40% 9) Cognitive impairment or active psychiatric condition 10) Inability to understand pain scoring 11) Emergency surgery 12) Re-do surgery 13) Re-exploration within 24 hours 14) Extubation after 6 hours of surgery

Design outcomes

Primary

MeasureTime frame
To assess the feasibility of opioid free anesthesia in coronary artery bypass surgeryTimepoint: 48 hours—

Secondary

MeasureTime frame
Adverse effects such as hyperalgesia , Postoperative nausea & vomiting, respiratory depression, pruritusTimepoint: 48 hours;Duration of mechanical ventilationTimepoint: 48 hours;Hemodynamic stability in the oerioperative periodTimepoint: 48 hours;Improvement in pulmonary function and oxygenationTimepoint: 48 hours—

Countries

India

Contacts

Public ContactDr NAVEEN G SINGH

Sri Jayadeva institute of Cardiovascular sciences and research

naveengsingh@hotmail.com9743950982

Outcome results

None listed

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