Effect of giving oral Pre-emptive Gabapentin for post operative pain relief to patients undergoing surgery under general anesthesia
Phase 4
- Conditions
- Health Condition 1: - Health Condition 2: O- Medical and Surgical
- Registration Number
- CTRI/2023/08/056640
- Lead Sponsor
- Pondicherry Institute of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
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
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.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To measure the efficacy of oral pre-emptive gabapentin in reducing post-operative <br/ ><br>pain when compared to placebo in patients undergoing surgery under general <br/ ><br>anaesthesia.Timepoint: 24 hours
- Secondary Outcome Measures
Name Time Method 1) Post operative total analgesic consumption for 24 hrs. <br/ ><br>2) Pre-operative anxiety between two groups. <br/ ><br>3) Intra-operative & post-operative hemodynamic changes (Heart rate, Mean arterial <br/ ><br>pressure) between two groups. <br/ ><br>4) Post operative sedation level between two groupsTimepoint: 24 hours