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Evaluation and Validation of Potential Risk Factors for Necrotizing Enterocolitis in Infants: A Combined Retrospective and Prospective Observational Study

Evaluation and Validation of Potential Risk Factors for Necrotizing Enterocolitis in Infants: A Combined Retrospective and Prospective Observational Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OOC-15005764
Enrollment
Unknown
Registered
2015-01-03
Start date
2015-01-15
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Neonatal necrotizing enterocolitis

Interventions

Sponsors

Neonatal Diagnosis and Treatment Center, Children's Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 1 Years

Inclusion criteria

Inclusion criteria: Section 1 (case-control study): case group: Patients with proven NEC through 2010/1 to 2015/1 in our Neonatal Ward. control group: Patients without NEC at the same time based on approximate conditions. Section 2(cohort study): exposed group: Patients with exposed factor through 2010/1 to 2015/1 in our Neonatal Ward.(e.g., congenital heart disease or sepsis) non-exposed group: Patients without the exposed factor at the same time based on approximate conditions.

Exclusion criteria

Exclusion criteria: Section 1 (case-control study): Hospitalized within 24h, shock, sepsis, systemic inflammatory response syndrome, gastrointestinal tract anomalies, genetic and metabolic disease. Section 2 (cohort study): Date of birth (shorter than 6 month difference), gestational age(shorter than 1 week apart)and birth weight (less than 100g difference)

Design outcomes

Primary

MeasureTime frame
Radiography;Clinical manifestation;

Countries

China

Contacts

Public ContactLu Qi
Qilu_qi@163.com+86 18580191965

Outcome results

None listed

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