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A real-world study of optimal enteral nutrition support protocols after intestinal surgery in infants

A real-world study of optimal enteral nutrition support protocols after intestinal surgery in infants

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300067996
Enrollment
Unknown
Registered
2023-02-02
Start date
2023-02-04
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

Intestinal atresia or stenosis, intestinal duplication malformation, intestinal perforation, etc.

Interventions

Enteral Nutrition Powder (AA-PA) group:N/A
Whole protein enteral nutrition preparations group:N/A

Sponsors

Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. children 0-6 months of age undergoing intestinal anastomosis (e.g. intestinal atresia or stricture, intestinal duplication malformation, intestinal perforation, etc.) 2. enteral nutritional support can be started within 48h after the operation. 3. the enteral nutrition preparation can be either amino acid-based enteral nutrition powder or whole protein-based enteral nutrition preparation 4. the child's parents or legal guardians (aged >=18 years) voluntarily sign the written informed consent.

Exclusion criteria

Exclusion criteria: 1. premature babies (<37 weeks of gestational age at birth) 2. very low birth weight children (<1500g). 3. children with other complications leading to gastrointestinal symptoms. 4. exclusively breastfed children. 5. children with contraindications to enteral nutrition (e.g. intestinal obstruction, severe shock, intestinal ischaemia, high-energy intestinal fistula, severe gastrointestinal bleeding, etc.). 6. children who have participated in other clinical studies within the last 3 months. 7. Other conditions that the investigator determines to be unsuitable for participation in this study.

Design outcomes

Primary

MeasureTime frame
Incidence of postoperative feeding intolerance in both groups;

Secondary

MeasureTime frame
Indicator of recovery of gastrointestinal function: time to full enteral nutrition;Changes in nutritional status;Length of stay in hospital;Anthropometric indicators: length, weight head circumference growth rate;Nutrition Risk Screening Score;Observed indicators of compliance;

Countries

Chian

Contacts

Public ContactFeng Jiexiong

Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology

fengjiexiong@126.com+86 139 8608 6129

Outcome results

None listed

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