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To study whether Nerve pain medicine, Gabapentin will reduce narcotic pain medicine requirement following heart surgery

Effect of Pre-emptive Gabapentin on Peri-operative Opioid Consumption in Patients Undergoing Coronary Artery Bypass Graft Surgery: A Randomized Controlled Double-Blinded Study - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/08/056487
Enrollment
80
Registered
2023-08-14
Start date
Unknown
Completion date
Unknown
Last updated
2023-08-21

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

Interventions

Intervention1: Gabapentin: 600mg 2 doses, 12 hours apart, on the night before and morning of surgery Control Intervention1: Placebo: 2 doses, 12 hours apart on the day before and morning of surgery Co

Sponsors

Anita Josprakash
Lead Sponsor
Dr Shibu C Kallivalappil
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1. Elective CABG 2. Same surgical and anaesthetic team 3. Beating Heart Surgeries 4. Age between 35 and 70 years 5. BMI less than 35kg/m2 6. Ejection Fraction greater than 30%

Exclusion criteria

Exclusion criteria: 1. Patient refusal to participate in the study 2. Patients with history of allergic reaction to gabapentin 3. Pregnant females 4. Patients posted for emergency surgeries, history of previous sternotomy or patients undergoing re-exploration sternotomy 5. Patients with history of comorbid diseases like neurological, psychiatric disorder or Alcohol dependence. 6. Patients with history of taking gabapentin or pregabalin in the past 3 months and chronic analgesic use, including opioids, NSAIDs or paracetamol etc. 7. Renal insufficiency (Serum Creatinine greater than 1.8)

Design outcomes

Primary

MeasureTime frame
1. To measure the opioid requirement intraoperatively & postoperatively 2. Pain scores at 0,1,3,6,12,24,36,48 & 72 hours after extubationTimepoint: 5 days

Secondary

MeasureTime frame
1) Postoperative Quality of Recovery. 2) Postoperative Nausea & vomiting. 3) Hyper-sedation. 4) Prolongation of mechanical ventilation.Timepoint: 5 days

Countries

India

Contacts

Public ContactDr Shibu C Kallivalappil

Jubilee Mission Medical College and Research Institute

drshibuck@yahoo.co.in9447078172

Outcome results

None listed

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