M40-M54
Conditions
Interventions
Group 1: Non-interventional study: retrospective survey arm 1, no intervention.
Sponsors
ulrich GmbH & Co. KG
Eligibility
Sex/Gender
All
Age
18 Years to 120 Years
Inclusion criteria
Inclusion criteria: 1. patient is at least 18 years old; 2. patient has undergone surgery with uBase in the period between 08/25/2015 and 05/31/2019; 3. patient is capable of recognizing the nature, significance, and scope of his or her decision to participate in the clinical clinical observational study and to direct his will accordingly; 4. an informed consent form dated and signed by the patient's own hand is available.
Exclusion criteria
Exclusion criteria: none
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint is postoperative improvement in the Core Outcome Measures Index (COMI). | — |
Secondary
| Measure | Time frame |
|---|---|
| - postoperative COMI back - postoperative back pain and leg pain on a numeric pain rating scale (NPRS; numeric pain rating scale) - fusion status at last routine check-up - Infra- and postoperative complications (especially implant- and procedure-related complications) | — |
Countries
Germany
Contacts
Public ContactMarcus Richter
St. Josefs Hospital
Outcome results
None listed