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Clinical Trials/EUCTR2009-018050-34-AT
EUCTR2009-018050-34-AT
Active, not recruiting
Not Applicable

Perioperative fluid management in patients receiving cadaveric renal transplants – Effects of normal saline versus balanced infusates on the incidence of electrolyte and acid-base disturbances

Medizinische Universität Wien,Univ.Klinik f.Anästhesie, Intensivmedizin und Schmerztherapie0 sitesMay 20, 2010
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Conditionspatients receiving cadaveric renal transplantation
DrugsPHYSIOLOGISCHE Kochsalzloesung Fresenius - InfusionsloesungELOMEL isoton - Infusionsloesung

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
patients receiving cadaveric renal transplantation
Sponsor
Medizinische Universität Wien,Univ.Klinik f.Anästhesie, Intensivmedizin und Schmerztherapie
Status
Active, not recruiting
Last Updated
13 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
May 20, 2010
End Date
TBD
Last Updated
13 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Sponsor
Medizinische Universität Wien,Univ.Klinik f.Anästhesie, Intensivmedizin und Schmerztherapie

Eligibility Criteria

Inclusion Criteria

  • •All patients with end\-stage\-renal disease admitted for cadaveric renal transplantation will be included in the study
  • •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) yes
  • •F.1\.3\.1 Number of subjects for this age range

Exclusion Criteria

  • •\-Patients younger than 18 years of age
  • •\-Hyperkalemia defined as a serum potassium exceeding 5\.5 mmol/L pre\-operatively

Outcomes

Primary Outcomes

Not specified

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