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A prospective multicenter randomized controlled study designed to assess the safety and efficacy of early enteral nutrition in neonatal intestinal anastomosis

A prospective multicenter randomized controlled study designed to assess the safety and efficacy of early enteral nutrition in neonatal intestinal anastomosis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-17014179
Enrollment
Unknown
Registered
2017-12-27
Start date
2018-01-02
Completion date
Unknown
Last updated
2018-01-08

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

Conditions

neonatal intestinal disformity

Interventions

Experimental group:early enteral nutrition
Control group:Routine treatment

Sponsors

Guangzhou Women and Children's Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 1 Years

Inclusion criteria

Inclusion criteria: All of the newborn who had the intestinal anastomosis operation

Exclusion criteria

Exclusion criteria: 1. accompany severe systemic infection before operation; 2. shock; 3. combined with fatal deformity.

Design outcomes

Primary

MeasureTime frame
post-operation hospital duration;—

Secondary

MeasureTime frame
complication rate (anastomotic leak ratep,eritonitis rate);cases requiring repeated gastrointestinal decompress;repeated NPO;time to start oral feeding;time to full-feeding;nutrition status (weight,length);—

Countries

China

Contacts

Public ContactYu Jiakang

Guangzhou Women and Children's Medical Center

jiakangyu@hotmail.com+86 13903058321

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 23, 2026