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Effect of giving oral Pre-emptive Gabapentin for post operative pain relief to patients undergoing surgery under general anesthesia

Efficacy of Oral Pre-emptive Gabapentin for post-operative pain relief in patients undergoing surgery under General Anaesthesia - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/08/056640
Enrollment
80
Registered
2023-08-18
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: - Health Condition 2: O- Medical and Surgical

Interventions

Intervention1: Tablet Gabapentin: oral gabapentin 600mg will be pre-medicated at two occasions, one at prior night & other at morning approximately 2 hours prior to shifting to OT for surgery. Contro

Sponsors

Pondicherry Institute of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1-Patients belonging to American Society of Anesthesiologist physical status classification I & II. 2-Patients aged between 18-65 years. 3-Patients scheduled for elective General Anesthesia procedures

Exclusion criteria

Exclusion criteria: 1-Patients undergoing Emergency surgical procedures. 2-Patients undergoing Surgeries under combined Regional/ Nerve blocks and General anesthesia 3-Patients undergoing laparoscopic surgeries. 4-Patients with history of chronic pain/prolonged pain medications. 5-Pregnant patients. 6-Patients with history of Psychiatric disease/ Drug abuse. 7-Patients with BMI > 40kg/m2. 8-Patients with history of use of anti-convulsant.

Design outcomes

Primary

MeasureTime frame
To measure the efficacy of oral pre-emptive gabapentin in reducing post-operative pain when compared to placebo in patients undergoing surgery under general anaesthesia.Timepoint: 24 hours

Secondary

MeasureTime frame
1) Post operative total analgesic consumption for 24 hrs. 2) Pre-operative anxiety between two groups. 3) Intra-operative & post-operative hemodynamic changes (Heart rate, Mean arterial pressure) between two groups. 4) Post operative sedation level between two groupsTimepoint: 24 hours

Countries

India

Contacts

Public ContactCheeranjeevi S

Pondicherry Institute of Medical Sciences

ramyavel1988@gmail.com9487630425

Outcome results

None listed

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