G35 G36
Conditions
Interventions
Group 1: Patients treated with tryptophan immunoadsorption for MS or NMO relapse during pregnancy or breastfeeding as part of their standard medical care will be documented.
Sponsors
Apherese Forschungsinstitut
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Relapse of multiple sclerosis or neuromyelitis optica during pregnancy and breastfeeding. Use of tryptophan immunoadsorption as escalation therapy.
Exclusion criteria
Exclusion criteria: Patient doesn´t agree to be treated. Treating physician doesn´t want to participate in the documentation.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Efficacy of tryptophan immunoadsorption for MS and NMO relapse in pregnant and breatfeeding patients by comparing clinical-neurological symptoms before and immediately after the immunodasorption series. | — |
Secondary
| Measure | Time frame |
|---|---|
| Tolerability and safety of tryptophan immunoadsorption. | — |
Countries
Germany
Contacts
Public ContactReinhard Klingel
Apherese Forschungsinstitut
Outcome results
None listed