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Clinical Analysis of Leukemoid Reaction in Very Low Birth Weight Infants Abstract

Clinical Analysis of Leukemoid Reaction in Very Low Birth Weight Infants Abstract

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600119857
Enrollment
Unknown
Registered
2026-03-04
Start date
2025-07-01
Completion date
Unknown
Last updated
2026-03-09

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

Conditions

Leukemoid reaction

Interventions

Experimental group:None
Control group:None

Sponsors

The First Affiliated Hospital of Zhengzhou University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Birth weight = 24 hours; 3.Infants born in other hospitals who were transferred to our hospital within 1 week after birth; 4.Meeting the diagnostic criteria for LR;

Exclusion criteria

Exclusion criteria: 1.congenital malformations; 2.admission age > 28 days; 3.incomplete clinical data;

Design outcomes

Secondary

MeasureTime frame
Condition of the amniotic fluid, placenta, and umbilical cord;—

Primary

MeasureTime frame
Incidence rate;Birth weight;—

Countries

China

Contacts

Public ContactTengfei Wang

The First Affiliated Hospital of Zhengzhou University

wangtf188@163.com+86 371 66862031

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 14, 2026