Clinical study on noninvasive central venous pressure in neonates

Status

Recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2300070617

Enrollment

Unknown

Registered

2023-04-18

Start date

2023-05-01

Completion date

Unknown

Last updated

2023-08-21

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

Conditions

Critically ill newborns and premature infants

Interventions

Group of critically ill newborns and premature infants:None

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Infants admitted to NICU; 2. Infants requiring UVC catheterization due to their condition; 3. Informed consent of legal guardian.

Exclusion criteria

Exclusion criteria: 1. Complex congenital heart disease; 2. Chromosome and genetic diseases.

Design outcomes

Primary

Measure	Time frame
Invasive central venous pressure;Inferior vena cava variability index, IVCVI;IVCmax/Ao;Inferior vena cava S/L;Tricuspid valve E/e’ ratio;	—

Countries

China

Contacts

Public ContactYiyong Fu

Chengdu Women’s and Children’s Central Hospital, School of Medicine, University of Electronic Science and Technology of China

xiaofoo000@126.com+86 15828063621

Outcome results

None listed

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