Description of Fluid Balance in Patients With Acute Respiratory Failure
Status unconfirmed
Conditions studied: Respiratory Insufficiency
In brief
The specific aim of this study is to gather data on fluid balance, intravenous medication administration, electrolyte balance, and diuretic and dialysis use in patients with acute respiratory failure who might benefit from a strategy designed to limit fluid administration.
Key facts
- Study ID
- NCT02523872
- Run by
- Smiths Medical, ASD, Inc.
- People needed
- 50
- Starts
- 2015-08-01
- Expected to finish
- 2015-12-01
- Last updated by the study team
- 2015-08-14
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Intubation and mechanical ventilation for ≤ 7 days
- An underlying condition associated with acute respiratory failure (e.g. pneumonia, ARDS, sepsis, asthma, COPD exacerbation)
- If in shock (MAP < 60, fluid bolus ≥30 ml/Kg or 4 L crystalloid or equivalent, vasopressors except for dopamine ≤ 5 mcg/kg/min or low-dose (≤ 0.04 IU/min) vasopressin) there should be no fluid bolus (1000 mL crystalloid or equivalent) for at least 12 hours
You may not qualify if…
- Intubation or mechanical ventilation for > 7 days
- Respiratory failure (requirement for positive pressure ventilation) in past 30 days
- Shock (MAP < 60, fluid bolus ≥30 ml/Kg or 4 L crystalloid or equivalent, vasopressors except for dopamine ≤ 5 mcg/kg/min or low-dose vasopressin) requiring fluid bolus (1000 mL crystalloid or equivalent) within past 12 hours
- Presence of a condition making it unlikely that the patient will be liberated from mechanical ventilation within the next 28 days (e.g. quadriplegia, end-stage lung disease, massive stroke, etc.)
- Prognosis from underlying condition ≤ 28 days (estimated 28 day mortality from underlying condition >50%)
- Likely intention (>50% probability) to withhold or withdraw life-supportive care within next 28 days
Where it is running
- University of Maryland Medical Center — Baltimore, Maryland, United States
Full record on ClinicalTrials.gov
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