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Initial worsening following initiation of rituximab therapy in patients with cryoglobulinemic vasculitis was described in 3.6% of cases. This worsening is often a serious condition, with high levels of mortality.
The objective of our study is to evaluate the efficacy of preventive plasmapheresis prior to the introduction of rituximab performed in Montpellier France since 2013 by assessing the frequency and severity of this flare effect in these patients compared to those reported in the literature.
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| Measure | Description | Time Frame |
|---|---|---|
| comparison of frequency of occurrence of flare effects | comparison of frequency of occurrence of flare effects between patients who received plasmapheresis prior to rituximab compared to patients who did not. | 1 day |
| Measure | Description | Time Frame |
|---|---|---|
| evaluation of the severity of the flare effect | evaluation of the severity of the flare effect | 1 day |
| impact of known risk factors | investigation of the impact of known risk factors for this effect |
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Inclusion criteria:
Exclusion Criteria:
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Adult patient with cryoglobulinemic vasculitis requiring rituximab treatment
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Charles HERBAUX, assistant Professor | Contact | 4 67 33 83 64 | 33 | c-herbaux@chu-montpellier.fr |
| Name | Affiliation | Role |
|---|---|---|
| Charles HERBAUX, assistant Professor | University Hospital, Montpellier | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Uhmontpellier | Recruiting | Montpellier | 34295 | France |
NC
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| ID | Term |
|---|---|
| C565141 | Cryoglobulinemia, Familial Mixed |
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| 1 day |
| evaluation of the safety of plasmapheresis in this indication | evaluation of the safety of plasmapheresis in this indication | 1 day |
| evaluation of the efficacy of plasmapheresis on biological parameters | evaluation of the efficacy of plasmapheresis on biological parameters | 1 day |