Predicting postoperative pain in patients undergoingsurgery for a degenerative spine disease usingpreoperative peak alpha frequency.

• Conditions: M53; M50; M51; M54; Cervical disc disorders; Other intervertebral disc disorders; Dorsalgia; Other dorsopathies, not elsewhere classified

• Registration Number: DRKS00032164
• Lead Sponsor: niversitätsmedizin Göttingen

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2023-07-03
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 80

Inclusion Criteria

Indication for surgical treatment of a degenerative
spine disease
• The patient is able to understand the nature,
significance and scope of the clinical study in the
context of patient information and to base the
decision to participate in the study on this.

Exclusion Criteria

Age < 18 years or >80 years
• Serious internal medicine/infectious disease
• Severe psychiatric illness
• Drug, alcohol or medication abuse

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Primary endpoint is pain rating measured by<br>numerical rating scale (zero to ten) at discharge.

Secondary Outcome Measures

Name	Time	Method
Secondary endpoints are:<br>1- Pain rating within 24 hours after surgery, <br>2- PAF, short-form McGill pain questionnaire, brief pain inventory, neuropathic pain scale at discharge <br>3- PAF, pain rating, shortform McGill pain questionnaire, brief pain inventory,<br>neuropathic pain scale, hospital anxiety, depression scale and EQ-5D-5L three months after surgery.