Inhaled NO in Surgical Patients With Recent COVID-19 Infection (INORDINATE)
Nitric Oxide, COVID-19, Surgery
About this trial
This is an interventional treatment trial for Nitric Oxide focused on measuring Nitric Oxide Inhalation, Postoperative Pulmonary Complications, Surgery, COVID-19
Eligibility Criteria
Inclusion Criteria: ≥ 18 years old Planned for surgery under general anesthesia With a history of COVID-19 infection within 7 weeks prior to surgery. Exclusion Criteria: Physician makes a decision that trial involvement is not in the patient's best interest or any condition that does not allow the protocol to be followed safely ASA ≥ IV, life expectancy< 24 h. Pregnant or lactating women. Severe liver disease (Child-Pugh score ≥ 12). Patients with severe respiratory failure need mechanical ventilation support or ECMO life support before the operation. Severe renal dysfunction (eGFRC≤30 ml/min/1.73m2) or receiving continuous renal replacement therapy, hemodialysis, and peritoneal dialysis. Having received or participated in other clinical trials within the previous month.
Sites / Locations
- Xijing HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Experimental: Treatment Group
Sham Comparator: Control Group
Inspired NO/N2 will be delivered at 80 parts per million (ppm) after anesthesia induction and intubation and lasted until the end of surgery and leave the operating room. The physician will follow their own institutional weaning protocols.
The delivery system will be set up anyway without studying gas administration