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| Sponsor: | Etablissement Français du Sang |
|---|---|
| Information provided by: | Etablissement Français du Sang |
| ClinicalTrials.gov Identifier: | NCT00235183 |
Purpose
The aim of the study is to compare the clinical efficacy of three types of plasma secured on the viral level either by quarantine or by chemical treatment in patients undergoing liver transplantation.
| Condition | Intervention | Phase |
|---|---|---|
|
Bleeding in Liver Transplantation |
Other: plasma |
Phase IV |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor) Primary Purpose: Treatment |
| Official Title: | Plasma Transfusion in Liver Transplantation : a Randomized, Double Blind, Multicenter Trial of Methylene Blue, Solvent/Detergent and Quarantined Plasma. |
| Estimated Enrollment: | 300 |
| Study Start Date: | June 2005 |
| Study Completion Date: | December 2010 |
| Primary Completion Date: | December 2009 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Active Comparator: Quarantined FFP
Quarantined FFP
|
Other: plasma
transfusion of more than 15 mL/Kg of plasma
|
|
Active Comparator: Methylene blue FFP
Methylene blue FFP
|
Other: plasma
transfusion of more than 15 mL/Kg of plasma
|
|
Active Comparator: Solvent detergent FFP
Solvent detergent FFP
|
Other: plasma
transfusion of more than 15 mL/Kg of plasma
|
Three types of plasma are transfused in bleeding patients undergoing liver transplantation:
In addition, the correction of coagulation abnormalities are studied.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| France | |
| EFS | |
| Paris, France, 75015 | |
| Principal Investigator: | Yves Ozier, MD, PhD | Hôpital Cochin, Paris, France |
| Principal Investigator: | Emmanuel Samain, MD, PhD | hôpital Jean Minjoz, Besançon, France |
| Principal Investigator: | Marie - Christine Gillon, MD | Hôpital Paul Brousse, Villejuif, France |
| Principal Investigator: | Loïc Villalon, MD | Hôpital Pontchaillou |
More Information
| Responsible Party: | President of EFS, Etablissement Français du Sang |
| ClinicalTrials.gov Identifier: | NCT00235183 History of Changes |
| Other Study ID Numbers: | EFS plasma trial |
| Study First Received: | October 6, 2005 |
| Last Updated: | July 1, 2011 |
| Health Authority: | France: Afssaps - French Health Products Safety Agency |
|
plasma bleeding liver transplantation |
|
Hemorrhage Pathologic Processes Methylene Blue |
Enzyme Inhibitors Molecular Mechanisms of Pharmacological Action Pharmacologic Actions |