Comparison of the effectiveness of Pregabalin with Pregabalin-Paracetamol on postoperative pai

Phase 3

Recruiting

• Conditions: Pain.; Other acute postprocedural pain; G89.18

• Registration Number: IRCT20141001019359N17
• Lead Sponsor: Bojnourd University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 1 May 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

Age between 20 to 60 years
ASA physical status I-II
Do not have drug addiction
Do not have allergic to Pregabalin and Paracetamol

Exclusion Criteria

If the patient have used paracetamol or pregabalin 48 hours before the operation.
If the patient be suffering from neurological and psychological, heart, lung, kidney and liver disease.
If the patient has any history of epilepsy.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain. Timepoint: Recovery, 12, 24 and 48 hours after surgery. Method of measurement: Visual Analog Score (VAS) Form of pain.

Secondary Outcome Measures

Name	Time	Method
Pregabalin and Paracetamol Side Effects. Timepoint: Up to 48 hours after surgery. Method of measurement: Examination and observation of the patient.