Immunoadsorption Versus Plasma Exchange for Treatment of Guillain-Barré Syndrome (GBS)
Recruiting now
Conditions studied: GBS
In brief
This is an observations study evaluating safety and efficacy of immunoadsorption compared to plasma exchange in Guillain-Barré Syndrome.
Key facts
- Study ID
- NCT04871035
- Run by
- University of Ulm
- People needed
- 20
- Starts
- 2021-04-28
- Expected to finish
- 2027-09-01
- Last updated by the study team
- 2026-05-01
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Diagnosis of Guillain-Barré Syndrome according to the diagnostic criteria proposed by Doorn et al. (Clinical features, pathogenesis, and treatment of Guillain-Barré syndrome, Lancet neurology 2008)
- age 18 years or above
You may not qualify if…
- Clinical or laboratory (C-reactive protein 20 mg/l or above, or evidence of nitrite-positive urinary tract infection) evidence of manifest systemic infection
- Intake of angiotensin converting enzyme inhibitor within1 weeks before first treatment
- Other contraindications against immunoadsorption or plasma exchange
Where it is running
- Department of Neurology, University of Ulm — Ulm, Baden-Wurttemberg, Germany (enrolling)
Full record on ClinicalTrials.gov
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