Efficacy of pregabalin in prevention of acute postoperative pain after oral surgery treatment

Phase 3

• Conditions: post-operative pain; R52.9; Pain, unspecified

• Registration Number: DRKS00005085
• Lead Sponsor: niveristy Hospital Dubrava, Department of Oral and Maxillofacial Surgery,

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2013-07-26
• Study Completion: 2015-03-10
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 71

Inclusion Criteria

Patients with anaesthesiologist's approval, classified in ASA 1 and ASA 2 group.

Exclusion Criteria

Patients with proven allergy to pregabalin, uncontrolled cardiovascular disease or diabetes, kidney disorders, liver disease, ones treated for chronic pain states, pregnant women and patients who took any analgesic 24 hours before the planned surgical treatment.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Visual analogue scale (VAS) will be used to measure the postoperative pain score, 2,6,12 and 24 hours after oral surgery treatments.

Secondary Outcome Measures

Name	Time	Method
Time and dose of rescue analgesics will be observed after a surgical treatment. Any of the side effects will be monitored and reported to the drug agency and manufacture representative.