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Effect of pregabalin on Total knee replacement post operative pai

Phase 3
Recruiting
Conditions
postoperative Pain
Total knee replacement
Anaesthesiology - Pain management
Registration Number
ACTRN12623001360606
Lead Sponsor
Bahrain defence forces hospital, royal medical services
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
120
Inclusion Criteria

1.Age between 21 to 85 year
2.Elective Regional anesthesia.
3.Able to follow study protocol

Exclusion Criteria

1.ASA -IV
2.Age <18 & > 85 years
3.Patients on pregabalin for chronic neuropathic pain.
4.Patient under General anesthesia
5.Patients with chronic liver failure
6.Patients with chronic renal failure on Hemodialysis
7.Patients on opioid (>3 month)
8.Patient with complicated knee surgery.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To measure Total Knee replacement Postoperative Pain by Visual Analogue Score 0-10[ Postoperative at 4hrs, 8hrs, 12hrs, 24hrs, 36 hrs, 48hrs, 60hrs, and 72hrs.]
Secondary Outcome Measures
NameTimeMethod
Sedation score[ Sedation score: RASS score postoperative at 4hrs, 8hrs, 12hrs, 24hrs, 36 hrs, 48hrs, 60hrs, 72hrs. <br>];Total Opioids consumption at 72 hrs<br>assessed from medical records of OPIODS Consumption, kept by nursing staff. [ post operative 72 hrs];Patient satisfaction at 72 hrs : rated as numeric 1-5 (1=not satisfied, 5=fully satisfied)<br>[ Postoperative 72 Hrs]
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