Status:

UNKNOWN

Hemodialysis Without Anticoagulation in Intensive Care Unit

Lead Sponsor:

Centre Hospitalier Départemental

Conditions:

Kidney Failure

Critically Ill

Eligibility:

All Genders

18+ years

Phase:

PHASE3

Brief Summary

The purpose of this study is to determine the safety and operative efficacy of intermittent hemodialysis without anticoagulation with saline flushes or Nephral 400ST in patients at high risk of bleedi...

Detailed Description

Hemodialysis in patients who are at high risk of bleeding complications represents a challenge of balancing the needs for establishment of an adequately functioning extracorporeal circuit for dialytic...

Eligibility Criteria

Inclusion

  • age \> 18 years
  • patient with high risk bleeding
  • patient requiring dialytic therapy in intensive care unit

Exclusion

  • Pregnancy
  • History of heparin-induced thrombocytopenia or serious heparin allergy
  • History of serious membrane dialysis allergy
  • Treatment by any of following medications 24H within the inclusion:
  • prophylactic or therapeutic anticoagulation with unfractioned heparin or low molecular weight heparin nonsteroidal anti-inflammatory agents direct thrombin inhibitors, antithrombin concentrate, activated protein C, anti-factor Xa pentasaccharide
  • Treatement by acetylsalicylic acid or other antiplatelet agent excluding platelet glycoprotein IIb/IIIa antagonists 7 days within the inclusion.

Key Trial Info

Start Date :

October 1 2005

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

April 1 2008

Estimated Enrollment :

120 Patients enrolled

Trial Details

Trial ID

NCT00242398

Start Date

October 1 2005

End Date

April 1 2008

Last Update

October 3 2007

Active Locations (1)

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CHD

La Roche-sur-Yon, France, 85925