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N/A N=11

Study Evaluating Liver Transplantation in Haemophilia Patients in Spain

Hemophilia · Hemophilia B

Enrolled (actual)
11
Serious AEs
Results posted
Jan 2013
Primary outcome: Primary: Number of Participants Requiring Immunosuppressive Therapy After Liver Transplantation — 7; 6; 4; 3 Participants

Study Design & Population

Study type
Observational
Phase
N/A
Interventions
Epidemiological Non interventional (Other)
Age
Pediatric, Adult, Older Adult
Sex
All
Sponsor
Wyeth is now a wholly owned subsidiary of Pfizer
Primary completion
Jun 2010

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants Requiring Immunosuppressive Therapy After Liver Transplantation
7; 6; 4; 3; 1
PRIMARY
Number of Participants With Acute Rejection of Liver Transplant
PRIMARY
Number of Participants With Hepatitis C Viral Infection Recurrence After Liver Transplantation
4
PRIMARY
Number of Participants Who Survived After Liver Transplantation
10
SECONDARY
Number of Participants Requiring Exogenous Clotting Factor Infusion During Liver Transplantation
5; 3
SECONDARY
Dose of Exogenous Clotting Factors Used During Liver Transplantation
62.88
SECONDARY
Number of Participants With and Without Hemophilia Requiring Immunosuppressive Therapy, Had Acute Rejection, Hepatitis C Viral Infection Recurrence and Who Survived After Liver Transplantation

Summary

This study will analyze survival and outcome of patients with severe haemophilia who undergo liver transplantation in Spain

Eligibility Criteria

Inclusion Criteria

  • Patients with haemophilia who underwent liver transplantation and who have been followed-up at any site in Spain.

Exclusion Criteria

  • Patients without informed consent form.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00927992). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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