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To determine the pre-emptive effect of Gabapentin on acute and chronic post-operative pain after spinal surgery

Phase 1
Conditions
Acute and chronic back pain after surgery
Registration Number
EUCTR2007-005996-32-GB
Lead Sponsor
uton & Dunstable Hospital NHS Foundation Trust
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Recruiting
Sex
Not specified
Target Recruitment
60
Inclusion Criteria

ASA I - 3 patients who underwent spinal operation in the age group of 18 - 75 years
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

Already on Gabapentin or allergy to Gabapentin or morphine

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Main Objective: To determine the pre-emptive effect of Gabapentin on patients who had spinal surgery;Secondary Objective: ;<br> Primary end point(s): Pain score for comparison of both groups.<br> Analgesia - Verbal Rates Score (VRS)<br> - LANSS assessment for neuropathic pain<br>
Secondary Outcome Measures
NameTimeMethod
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