The neonatal asphyxia and intestinal microflora

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2000030122

Enrollment

Unknown

Registered

2020-02-23

Start date

2020-03-01

Completion date

Unknown

Last updated

2020-02-25

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

Conditions

the neonatal asphyxia

Interventions

asphyxia group:N/A

non asphyxia group:N/A

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Exposure group: 1. gestational age 37w-42w live newborn; 2. accord with diagnostic criteria of neonatal asphyxia; 3. receive permission from guardian; 4. finish follow-up study. No exposure group: 1. healthy newborn; 2. receive permission from guardian; 3. finishi follow-up study.

Exclusion criteria

Exclusion criteria: Exposure group: 1. live time < 72 hours because of serious station; 2. give up therapy. Non-exposure group: no exclusion criteria.

Design outcomes

Primary

Measure	Time frame
intestinal microflora;	—

Secondary

Measure	Time frame
growth and development;	—

Countries

China

Contacts

Public ContactHan Ying, Hou Xinlin

Peking University First Hospital

houxinlin66@163.com+86 13661013288

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026