Neonatology Clinical Trial
Official title:
Optimization and Clinical Study of Early Prediction Model for Neonatal Acute Respiratory Distress Syndrome
| NCT number | NCT05647850 |
| Other study ID # | 123456 |
| Secondary ID | |
| Status | Recruiting |
| Phase | |
| First received | |
| Last updated | |
| Start date | January 1, 2023 |
| Est. completion date | December 31, 2025 |
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.
| Status | Recruiting |
| Enrollment | 2000 |
| Est. completion date | December 31, 2025 |
| Est. primary completion date | December 1, 2025 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | All |
| Age group | 1 Minute and older |
| Eligibility | 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 |
| Country | Name | City | State |
|---|---|---|---|
| China | University-Town Hospital of Chongqing Medical University | Chongqing | Chongqing |
| China | Women and Children's Hospital of Chongqing Medical University | Chongqing | Chongqing |
| Lead Sponsor | Collaborator |
|---|---|
| University-Town Hospital of Chongqing Medical University |
China,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | General characteristics of the patients | 2023.1-2025.12 |
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