Coagulation Disorders Secondary to Two Plasmapheresis Techniques (Double Filtration Plasmapheresis vs. PFS). Descriptive Pilot Study.

Recruiting N/A Interventional Study
Hyperfibrinogenemia Hemostatic Disorder
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Health Services Research
Participants needed
6 (estimated)
Sponsor
Centre Hospitalier Universitaire de Nīmes · Other
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About This Trial
Therapeutic plasmapheresis causes changes in haemostasis by purifying many of the circulating factors involved. Few reliable data are available on these changes and most studies are limited to coagulation factor assays before and after the session, with little data documenting the kinetics of regeneration of these factors. It is recognized that haemostasis disorders caused by therapeutic apheresis…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Patients without renal failure treated with chronic therapeutic plasmapheresis with a minimum treatment interval of 10 days and who can be treated with single plasma exchange (SPE) or double filtration plasmapheresis (DFPP) in accordance with the international recommendations.…
Contacts

Olivier MORANNE, Professor

+334.66.68.31.49

olivier.moranne@chu-nimes.fr

CONTACT

Anissa MEGZARI

+33466684236

drc@chu-nimes.fr

CONTACT