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Safety and efficacy study of a nitric oxide generating system for neonatal cannulation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN96341949
Enrollment
Unknown
Registered
2004-09-30
Start date
2003-08-01
Completion date
Unknown
Last updated
2015-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neonatal Diseases: Cannulation Neonatal Diseases Cannulation

Interventions

1. Nitric oxide for neonatal cannulation 2. No nitric oxide

Sponsors

Record Provided by the NHSTCT Register - 2004 Update - Department of Health (UK)
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Neonates presenting to neonatal intensive care unit (NICU)

Exclusion criteria

Exclusion criteria: Not provided at time of registration

Design outcomes

Primary

MeasureTime frame
Increased success in percutaneous long line placement in neonates—

Secondary

MeasureTime frame
Not provided at time of registration—

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026