Strength Testing After Nitrate Delivery (STAND) in ICU Patients
Respiratory Failure
About this trial
This is an interventional treatment trial for Respiratory Failure focused on measuring ICU, Respiratory Failure, Weakness, Nitrate supplementation
Eligibility Criteria
Inclusion Criteria:
- Age > 55 years
- Mechanically ventilated via an endotracheal tube or mask who have begun spontaneous breathing trials or extubated within the previous 24 hours
- Lung Injury as defined by a PaO2 / FiO2 < 300
Exclusion Criteria:
- Inability to walk without assistance prior to acute ICU illness (use of a cane or walkers not exclusions)
- Cognitive impairment prior to acute ICU illness (non-verbal)
- Acute stroke
- Body mass index (BMI) >50
- Neuromuscular disease that could impair weaning (myasthenia gravis, ALS, Guillain-Barre)
- Hip fracture, unstable cervical spine or pathological fracture
- Mechanically Ventilated > 80 hours
- Current hospitalization or transferring hospital stay > 7 days
- DNR/DNI on admission
- Cancer treatment within the last 6 months
- Moribund
- Participation in another research study
- On nitroglycerine or nitrate preparations used with angina or phosphodiesterase type 5 inhibitors
- Body mass less than 60 kg
Sites / Locations
- Wake Forest University Health Sciences
Arms of the Study
Arm 1
Arm 2
Experimental
Placebo Comparator
Nitrate Rich
Nitrate Depleted
A nitrate rich beetroot juice supplement (Beet It Shot®, James White Drinks, UK) high in nitrates will be provided to the subjects. Subject's diet will be supplemented once daily while hospitalized up to 14 days with one 70 ml bottle containing 300 mg of dietary nitrate.
This group will consume a beetroot juice supplement (Beet It Shot®, James White Drinks, UK) that has had the nitrate removed from the beverage by the manufacturer. Patient's diet will be supplemented once daily with one 70 ml bottle while hospitalized up to 14 days.