Optimization and Clinical Study of Early Prediction Model for Neonatal Acute Respiratory Distress Syndrome

Status

UNKNOWN

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT05647850

Enrollment

2000

Registered

2022-12-13

Start date

2023-01-01

Completion date

2025-12-31

Last updated

2023-11-07

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

Conditions

Neonatology

Keywords

Neonatal acute respiratory distress syndrome, Model of prediction, Perinatal factors

Brief summary

The goal of this observational study is to learn about neonatal acute respiratory distress syndrome in describe participant population. The main question it aims to answer is: using perinatal factors to predict early neonatal acute respiratory distress syndrome and reduce its mortality. Participants' umbilical cord blood will be collected for testing, but will not receive any intervention.

Interventions

OTHERNo intervention

No intervention

Study design

Observational model

CASE_CONTROL

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

1 Minutes to No maximum

Healthy volunteers

Yes

Inclusion criteria

* A newborn born alive

Exclusion criteria

* Stillborn newborn * Respiratory distress syndrome(RDS), transient tachypnoea of the neonate (TTN), or congenital anomalies as a primary current acute respiratory condition * Hereditary endocrine and metabolic diseases * Incomplete records

Design outcomes

Primary

Measure	Time frame
General characteristics of the patients	2023.1-2025.12

Countries

China

Contacts

Primary ContactHui Liu

liuhui8805@126.com+8615223013501

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026