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
Recruiting now · Not applicable
Conditions studied: ARDS
In brief
Investigating the Impact of Combined Inhaled Nitric Oxide and Prone Positioning on the Efficacy in ARDS Patients
Key facts
- Study ID
- NCT06741137
- Run by
- Northern Jiangsu People's Hospital
- People needed
- 30
- Starts
- 2024-01-01
- Expected to finish
- 2025-12-31
- Last updated by the study team
- 2025-01-10
Who can join
Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age 18-80 years;
- Patients with moderate to severe ARDS on mechanical ventilation
You may not qualify if…
- 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.
- Mid to late pregnancy.
- Patients with a history of malignancy or other irreversible diseases/conditions, including those in the terminal stage.
- Patients expected to be discharged soon or requiring invasive mechanical ventilation for less than 24 hours.
- Patients currently participating in other studies.
Where it is running
- Northern Jiangsu People's Hospital — Yangzhou, Jiangsu, China (enrolling)
Full record on ClinicalTrials.gov
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