Actively Recruiting

Age: 18Years - 80Years
All Genders
NCT06680895

FeNO Observation Study in ICU Patients With ARS

Led by Shanghai Zhongshan Hospital · Updated on 2024-11-08

1000

Participants Needed

1

Research Sites

78 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

1. Main Objective: To compare the concentration of exhaled nitric oxide in patients with different severity of respiratory failure in ICU. 2. Secondary Purpose: 1. To observe the change of nitric oxide concentration in exhaled breath of patients with mechanical ventilation over time; 2. The relationship and differences between pulmonary ventilation blood flow levels in patients with different exhaled NO concentrations; 3. Reactivity of patients with different exhaled NO concentrations to inhaled nitric oxide therapy and the relationship between them.

CONDITIONS

Official Title

FeNO Observation Study in ICU Patients With ARS

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patients (≥18 years of age) with mechanical ventilation or advanced respiratory support in the ICU, regardless of gender
  • Expected mechanical ventilation time of tracheal intubation is more than 24 hours
  • Initial ventilator settings: oxygen fraction (FIO2) = 50%, respiratory rate = 15/min, positive end-expiratory pressure (PEEP) = 5 cmH2O, tidal volume = 6-8 ml/kg ideal body weight (IBW), inspiration-exhalation ratio = 1:2
  • Agree to participate and sign informed consent
Not Eligible

You will not qualify if you...

  • Use of any nitric oxide containing drugs, anti-inflammatory drugs, or drugs affecting airway diameter within 6 hours before the first FeNO measurement
  • Participation in other clinical research projects
  • Patients deemed unsuitable by the investigators

AI-Screening

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Trial Site Locations

Total: 1 location

1

Shanghai Zhongshan hospital

Shanghai, Shanghai Municipality, China, 200030

Actively Recruiting

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Research Team

H

Huan Wang, Master

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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