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amotrigine vs Pregabalin for postoperative pain relief in Spine Surgeries

Not Applicable
Conditions
Health Condition 1: S320- Fracture of lumbar vertebra
Registration Number
CTRI/2020/08/027307
Lead Sponsor
IMS BH
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Patients undergoing spine surgery under general anaesthesia

ASA physical status- I / II

Exclusion Criteria

ASA III/IV

Pregnancy/Lactation

Patient with epilepsy

Impaired liver functions/renal functions

H/O drug abuse/ Alcohol abuse

Allergy to pregabalin or lamotrigine

H/O vertigo

Intake of corticosteroids

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Visual Analogue Score for PainTimepoint: 1,2,4 and 6 hours
Secondary Outcome Measures
NameTimeMethod
Dosage of analgesia requiredTimepoint: 1,2,4 and 6 hours
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