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

U

University-Town Hospital of Chongqing Medical University

Status

Enrolling

Conditions

Neonatology

Treatments

Other: No intervention

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

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.

Enrollment

2,000 estimated patients

Sex

All

Ages

1+ minute old

Volunteers

Accepts Healthy Volunteers

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

Trial design

2,000 participants in 2 patient groups

Baseline characteristics of all patients
Treatment:
Other: No intervention
General characteristics of the patients.
Treatment:
Other: No intervention

Trial contacts and locations

2

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Central trial contact

Hui Liu

Data sourced from clinicaltrials.gov

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