A Prospective, Open, Single-arm, Multi-center Phase IV Clinical Study of Inhaled Nitric Oxide Combined With Ventilatory Support for the Treatment of Neonatal (Gestational Age ≥34 Weeks) Hypoxic Respiratory Failure With Pulmonary Hypertension.

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Observational
SUMMARY

This is a prospective, open-label, single-arm, multicenter Phase IV clinical study to evaluate the safety of INOmax for the treatment of hypoxic respiratory failure with pulmonary hypertension in newborns (≥ 34 weeks gestational age). To evaluate the safety of INOmax combined with ventilatory support in the treatment of neonatal (≥ 34 weeks gestational age) hypoxic respiratory failure with pulmonary hypertension.

Eligibility
Participation Requirements
Sex: All
Maximum Age: 7 days
Healthy Volunteers: f
View:

• Neonates ≥ 34 weeks gestation age.

• Hypoxic respiratory failure requiring more than 24 hours of ventilatory support.

• Clinical or echocardiographic evidence of pulmonary hypertension (systolic pulmonary arterial pressure \[sPAP\] \> 35 mm Hg or \> 2/3 systemic blood pressure \[SBP\] or there is a right-to-left shunt at the atrium or arterial ductus).

• Age less than 7 days at the time of treatment initiation with study drug.

• The neonatal guardian agrees to participate in the study and signs an informed consent form (ICF).

Locations
Other Locations
China
Guangzhou Women and Children'S Medical Center
RECRUITING
Guangzhou
Contact Information
Primary
Wen hao Zhou
zwhchfu@126.com
+86-18017591123
Time Frame
Start Date: 2024-12-12
Estimated Completion Date: 2026-12-30
Participants
Target number of participants: 120
Treatments
inhaled nitric oxide combined with ventilatory support
Sponsors
Leads: Lee's Pharmaceutical Limited

This content was sourced from clinicaltrials.gov