Isotonic Solution Administration Logistical Testing
Status: | Completed |
---|---|
Conditions: | Renal Impairment / Chronic Kidney Disease |
Therapuetic Areas: | Nephrology / Urology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 4/21/2017 |
Start Date: | February 2015 |
End Date: | June 2015 |
Isotonic Solution Administration Logistical Testing: Pilot Study for the Isotonic Solutions and Major Adverse Renal Events Trial
The administration of intravenous crystalloids is ubiquitous in the care of the critically
ill. Commonly available crystalloid solutions contain a broad spectrum of electrolyte
compositions including a range of chloride concentrations. Recent studies of associated
higher fluid chloride content with acute kidney injury and mortality but no large,
randomized trials have been conducted. In preparation for a large, cluster-randomized,
multiple-crossover trial comparing 0.9% sodium chloride to physiologically-balanced isotonic
crystalloids (Lactated Ringers or Plasmalyte-A) in intensive care unit patients, this pilot
study will enroll all patients admitted to the medical intensive care unit at a single
tertiary center for a sixth month period. The primary objective will be to test the ability
of an electronic order entry tool to ensure administration of assigned study fluid or record
contraindications to assigned study fluid. The pilot study will also demonstrate the
feasibility of collecting demographic, severity of illness, fluid management, vital sign,
laboratory, acute kidney injury and renal replacement therapy, and outcome data in an
automated, electronic fashion.
ill. Commonly available crystalloid solutions contain a broad spectrum of electrolyte
compositions including a range of chloride concentrations. Recent studies of associated
higher fluid chloride content with acute kidney injury and mortality but no large,
randomized trials have been conducted. In preparation for a large, cluster-randomized,
multiple-crossover trial comparing 0.9% sodium chloride to physiologically-balanced isotonic
crystalloids (Lactated Ringers or Plasmalyte-A) in intensive care unit patients, this pilot
study will enroll all patients admitted to the medical intensive care unit at a single
tertiary center for a sixth month period. The primary objective will be to test the ability
of an electronic order entry tool to ensure administration of assigned study fluid or record
contraindications to assigned study fluid. The pilot study will also demonstrate the
feasibility of collecting demographic, severity of illness, fluid management, vital sign,
laboratory, acute kidney injury and renal replacement therapy, and outcome data in an
automated, electronic fashion.
Inclusion Criteria:
- Admitted to the adult medical intensive care unit (MICU) at Vanderbilt University
Medical Center
Exclusion Criteria:
- Age<18 years old
We found this trial at
1
site
1211 Medical Center Dr
Nashville, Tennessee 37232
Nashville, Tennessee 37232
(615) 322-5000
Vanderbilt Univ Med Ctr Vanderbilt University Medical Center (VUMC) is a comprehensive healthcare facility dedicated...
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