A Pilot Study of the Effect of the Combination of Inhaled Nitric Oxide and Prone Position Under EIT Monitoring on Efficacy in Patients with ARDS

ConditionARDS
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-80
SponsorNorthern Jiangsu People's Hospital

About this trial

Investigating the Impact of Combined Inhaled Nitric Oxide and Prone Positioning on the Efficacy in ARDS Patients

Eligibility criteria

Qualifiers

Age 18-80 years;

Patients with moderate to severe ARDS on mechanical ventilation

Disqualifiers

Patients with severe asthma or acute exacerbation of chronic obstructive pulmonary disease (COPD), lung tumors, post-lung resection, and post-lung transplantation.

Patients with hemodynamic instability requiring vasopressor support: dopamine or dobutamine >15 µg/kg/min, norepinephrine >0.3 µg/kg/min.

Cardiogenic pulmonary edema.

Patients with severe facial deformities, facial trauma, or severe thoracoabdominal trauma that precludes prone positioning ventilation.

Trial design

Treatments tested in this trial

  • inhaled nitric oxide combined with prone position ventilation

Treatment groups

30 Participants
are divided into 1 treatment group