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PROSTACYCLIJN VERSUS HEPARIN AS ANTICOAGULANT IN CONTINUOUS VENO-VENOUS HEMODIAFILTRATION - ND

Conditions
Acute renale failure in intensive unit
MedDRA version: 9.1Level: LLTClassification code 10038436Term: Renal failure acute
Registration Number
EUCTR2007-004426-24-IT
Lead Sponsor
POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Recruiting
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

Patient with acute renal failure admitted to the Intensive Care Unit of our hospital requiring renal replacement therapy according to the latest international guidelines
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

H.they do not fulfil the inclusion criteria
I.they are less than 18 years old
J.they are pregnant women
K.they have been treated with another experimental drug or device within 30 days before the admission to the present study
L.they are positive to HIV infection
M.they have been presenting an haemorrhage in the la test 24 hours
N.they are thrombocytopenic (platelets count less than 30,000 cells/mm3)

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Main Objective: to verify the feasibility and efficacy of prostacyclin versus heparin as antihemostatic agent during veno-venous hemodiafiltration (CVVHDF).;Secondary Objective: Monitoring effects of PROSTACYCLIJN on th platelets;Primary end point(s): nd
Secondary Outcome Measures
NameTimeMethod
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