Skip to main content
Clinical Trials/ISRCTN76588266
ISRCTN76588266
Completed
未知

Randomised comparison of fluid resuscitation with human albumin solution or normal saline among critically ill patients

The George Institute for International Health (Australia)0 sites7,000 target enrollmentSeptember 19, 2002

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
The George Institute for International Health (Australia)
Enrollment
7000
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

Registry
who.int
Start Date
September 19, 2002
End Date
December 31, 2004
Last Updated
3 years ago
Study Type
Interventional

Investigators

Sponsor
The George Institute for International Health (Australia)

Eligibility Criteria

Inclusion Criteria

  • Patients are eligible for inclusion in the study if ALL the following requirements are met:
  • 1\. Fluid resuscitation is required for intravascular fluid depletion that is in addition to intravenous fluid that is required for nutrition or to replace ongoing insensible losses, urinary losses, ongoing losses from other sites (e.g., fistula losses from the gastrointestinal tract, urinary losses from diabetes insipidus, cerebral salt wasting syndrome or the polyuric phase of acute renal failure) or to restore normonatraemia
  • 2\. The ICU clinician considers that both 4% human albumin solution and 0\.9% sodium chloride are equally appropriate for the patient and that no specific indication or contraindication for either exists
  • 3\. The requirement for fluid resuscitation must be supported by AT LEAST ONE of the following clinical signs:
  • a. Heart rate greater than 90 beats/min
  • b. Systolic Blood Pressure (SBP) less than 100 mmHg or Mean Arterial Pressure (MAP) less than 75 mmHg or a 40 mmHg decrease in SBP or MAP from the baseline recording
  • c. Central venous pressure less than 10 mmHg
  • d. Pulmonary artery wedge pressure less than 12 mmHg
  • e. Respiratory variation in systolic or mean arterial blood pressure of greater than 5 mmHg
  • f. Capillary refill time greater than one second

Exclusion Criteria

  • Patients are excluded from the study if one or more of the following are present:
  • 1\. A known previous adverse reaction to human albumin solution
  • 2\. Any known religious objection to the administration of human blood products (for example if patient is a Jehovah?s Witness)
  • 3\. A requirement for the patient to receive plasmapheresis during this ICU admission
  • 4\. An admission to the ICU following cardiac surgery
  • 5\. An admission to the ICU for the treatment of body burn
  • 6\. An admission to the ICU following liver transplantation surgery
  • 7\. Age less than 18 years
  • 8\. Brain death or brain death that is likely to be diagnosed within in the next 24 hours of fluid resuscitation being required
  • 9\. If the patient is moribund and expected to die within the next 24 hours \- defined as having a treatment limitation order in place that exceeds a ?not for resuscitation? order and that indicates the treating clinicians are not committed to full supportive care

Outcomes

Primary Outcomes

Not specified

Similar Trials