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

Recruiting

• Conditions: Neonatology
• Interventions: Other: No intervention

• Registration Number: NCT05647850
• Lead Sponsor: University-Town Hospital of Chongqing Medical University

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.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2022-11-30
• Study First Submitted QC: 2022-11-30
• Study First Posted: 2022-12-13
• Study Start: 2023-01-01
• Status Verified: 2023-11
• Last Update Submitted: 2023-11-06
• Last Update Posted: 2023-11-07
• Primary Completion: 2025-12-01
• Study Completion: 2025-12-31

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 2000

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

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Baseline characteristics of all patients	No intervention	-
General characteristics of the patients.	No intervention	-

Primary Outcome Measures

Name	Time	Method
General characteristics of the patients	2023.1-2025.12

Trial Locations

Locations (2)

University-Town Hospital of Chongqing Medical University; 🇨🇳 Chongqing, Chongqing, China

Women and Children's Hospital of Chongqing Medical University; 🇨🇳 Chongqing, Chongqing, China