Diagnoses which lead to spine surgery
Conditions
Interventions
Group 1: Patients undergoing back surgery
The following assessments and measurements are carried out as part of this study:
-Screening (7 days before surgery)
-->Informed consent, verification of ful
Sponsors
UKE Universitätsklinikum Hamburg Eppendorf
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients undergo spinal surgery at the university clinic Hamburg Eppendorf, sufficient proficiency in German
Exclusion criteria
Exclusion criteria: non sufficient proficiency in German, Patient is unable to give consent (e.g. incompliance or dementia), Back pain due to a tumour
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Difference score pre-postoperative of pain on a numerical rating scale (NRS) 0-10 (0 = no pain, 10 = the worst pain imaginable) | — |
Secondary
| Measure | Time frame |
|---|---|
| Treatment expectations Questionnaires: self generated expectancy questionnaire; SBI; SETS; ASES Dates at which data is collected; pre-operational, 2 & 4 days post operational Follow Up (3 Months post OP) | — |
Countries
Germany
Contacts
Public ContactRegine Klinger
Bereich Schmerzmedizin und SchmerzpsychologieUniversitätsklinikum Hamburg-Eppendorf (UKE)?Zentrum für Anästhesiologie und Intensivmedizin?Klinik und Poliklinik für Anästhesiologie
Outcome results
None listed