G70.0
Conditions
Interventions
Group 1: Tmin: MG patients who underwent minimally invasive thymectomy
Group 2: Toffen: MG patients who underwent an open thymectomy
Group 3: T0: MG patients who did not undergo a thymectomy
Sponsors
Charité Universitätsmedizin Berlin
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: - Confirmed diagnosis of MG - Capacity to consent and written informed consent of the patient - Minimally invasive thymectomy performed = 90 days ago (Tmin group) or open thymectomy = 90 (Toffen group) OR - No thymectomy (T0 group)
Exclusion criteria
Exclusion criteria: - Lack of communication skills
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Survival time after 5 years | — |
Secondary
| Measure | Time frame |
|---|---|
| Taking steroid therapy (yes/no) Average daily steroid dose Use of long-term immunosuppression (includes use of azathioprine, mycophenolate mofetil, methotrexate, ciclosporin, rituximab, efgartigimod or ravulizumab) Use of exacerbation therapy [plasmapheresis / immunoadsorption / intravenous immunoglobulins (IVIG)] Myasthenia Gravis Activities of Daily Living (MG-ADL) scale Occurrence of a perioperative complication (e.g. injury to neighboring organs and structures, bleeding, etc.) New occurrence of other autoimmune diseases after thymectomy (e.g. systemic lupus erythematosus (SLE), rheumatoid arthritis (RA), etc.). | — |
Countries
Germany
Contacts
Public ContactFrauke Stascheit
Charité Universitätsmedizin Berlin
Outcome results
None listed