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Clinical Trials/NCT00609700
NCT00609700
Completed
Not Applicable

Balanced Volume Replacement Therapy With Ringer's Acetate Solution in Burn Injury

Klinikum St. Georg gGmbH1 site in 1 country82 target enrollmentDecember 2007

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Severe Burn Injury
Sponsor
Klinikum St. Georg gGmbH
Enrollment
82
Locations
1
Primary Endpoint
Change of SOFA-score from day 3 to day 7 after severe burn injury
Status
Completed
Last Updated
14 years ago

Overview

Brief Summary

This observational study compares the influence of Ringer's Lactate solution and Ringer's Acetate solution on organ function scores following severe burn injury.

Detailed Description

In the early period following severe burn injury volume replacement with high amounts of crystalloids is necessary. In this study we compare the organ function scores of a historical patient group, treated with Ringer's Lactate solution, with an actual patient population, treated with Ringer's Acetate solution.

Registry
clinicaltrials.gov
Start Date
December 2007
End Date
December 2010
Last Updated
14 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Armin Sablotzki, MD

prof. Dr. med.

Klinikum St. Georg gGmbH

Eligibility Criteria

Inclusion Criteria

  • Age \>=18 years and \<80years
  • Burned surface area \>20% and \<70%
  • Burn injury \< 24 hours
  • Agreement to the study procedures

Exclusion Criteria

  • Burned surface area \> 70%
  • Expected survival time \< 24 hours
  • Acute or chronic heart failure NYHA III or IV
  • Adult respiratory distress syndrome
  • Renal failure
  • Hepatic failure

Outcomes

Primary Outcomes

Change of SOFA-score from day 3 to day 7 after severe burn injury

Time Frame: day3, day7, day28, day60

Secondary Outcomes

  • Changes in electrolyte-balance(day3, day7, day28)

Study Sites (1)

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