Actively Recruiting
A Real-world Study of Nitric Oxide Generator and Delivery System
Led by Novlead Inc. · Updated on 2025-02-19
10
Participants Needed
1
Research Sites
121 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The study is aimed to observe the efficacy and safety of Nitric Oxide Generator and Delivery System in Pulmonary Hypertension of Newborn in real clinical settings.
CONDITIONS
Official Title
A Real-world Study of Nitric Oxide Generator and Delivery System
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Clinically considered to benefit from inhaled nitric oxide (iNO) and decided to use Nitric Oxide Generator and Delivery System by clinicians
- Admitted to the Department of Neonatology at the hospital, gender unlimited
- Diagnosed as pulmonary hypertension and undergoing or decided to undergo respiratory support
- Documented Oxygenation index (OI) 258 prior to the treatment
- Signed informed consent by the parent(s) or the legal representative(s) with full awareness of the benefits and risks of this study
You will not qualify if you...
- Proven risks of nitric oxide contraindication
- Undergoing or expected to need a combination of other pulmonary vasodilators, surfactants or extracorporeal membrane oxygenation
- Other circumstances that investigators believe unsuitable for enrollment
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
ZhuJiang Hospital of Southern Medical University
Guangzhou, Guangzhou, China
Actively Recruiting
Research Team
Z
Zhou Fang
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
1
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