Skip to content

A randomized controlled trial of nutritional strategies in asphyxia neonates during mild hypothermia

A randomized controlled trial of nutritional strategies in asphyxia neonates during mild hypothermia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100048890
Enrollment
Unknown
Registered
2021-07-19
Start date
2021-07-15
Completion date
Unknown
Last updated
2022-09-26

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

Conditions

Neonatal asphyxia

Interventions

Experimental Group:Entera feeding
Control Group:No feeding

Sponsors

Chengdu Women and Children's Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Gestational age> 36 weeks, birth weight> 2500g; 2. Perinatal asphyxia occurred and neonatal resuscitation was received; 3. Neonatal hypoxic-ischemic encephalopathy (HIE) has been diagnosed with moderate to severe; 4. No substandard Hypothermia and feeding contraindications, accept mild hypothermia treatment; 5. Parents sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with incomplete clinical data; 2. Sub-hypothermia treatment or nutritional support has been performed in the outside hospital at the time of admission; 3. Intracranial hemorrhage, pulmonary hemorrhage and other cavities and organs bleeding or bleeding tendency; 4. Abnormal coagulation function or platelets <50x10^9/L; 5. Vomiting, abdominal distension, weakened or disappeared bowel sounds, gastrointestinal bleeding.

Design outcomes

Primary

MeasureTime frame
neonatal enterocolitis;

Countries

China

Contacts

Public ContactHu Xuhong

Chengdu Women and Children's Central Hospital

1404351037@qq.com+86 13881850909

Outcome results

None listed

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