Predicting postoperative pain in patients undergoing surgery for a degenerative spine disease using preoperative peak alpha frequency.

Predicting postoperative pain in patients undergoing surgery for a degenerative spine disease using preoperative peak alpha frequency. - Predictpain

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00032164

Enrollment

Registered

2023-07-03

Start date

2023-08-24

Completion date

Unknown

Last updated

2026-01-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

M50 M51 M54 M53

Interventions

Group 1: Patients who are surgically treated for a degenerative spine disease.

Eligibility

Sex/Gender

All

Age

18 Years to 80 Years

Inclusion criteria

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

Exclusion criteria: Age 80 years • Serious internal medicine/infectious disease • Severe psychiatric illness • Drug, alcohol or medication abuse

Design outcomes

Primary

Measure	Time frame
Primary endpoint is pain rating measured by numerical rating scale (zero to ten) at discharge.	—

Secondary

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

Countries

Germany

Contacts

Public ContactTammam Abboud

Universitätsmedizin Göttingen

tammam.abboud@med.uni-goettingen.de+49 551 39 65246

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026