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A prospective, observational, multicentric study to assess the effectiveness and safety of short peptide enteral nutrition in critically ill patients

A prospective, observational, multicentric study to assess the effectiveness and safety of short peptide enteral nutrition in critically ill patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500103018
Enrollment
Unknown
Registered
2025-05-22
Start date
2025-06-01
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

None

Interventions

Observation group:None

Sponsors

Zhejiang Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1 Age: >= 18 years old, 2 Admit to ICU with invasive mechanical ventilation, 3 Patients are suitable for using short peptide enteral nutrition as complete nutrition for at least 3 days, 4 Agree to participate in this study and signed the informed consent.

Exclusion criteria

Exclusion criteria: 1 Patients of advanced cancer cachexia and disease-specific cachexia, 2 Patients with severe hepatic and renal dysfunction, 3 Patients who are pregnant or breast feeding, 4 Patients who are participating in another trial, 5 Patients who are using parenteral nutrition.

Design outcomes

Primary

MeasureTime frame
Prealbumin change ;—

Countries

China

Contacts

Public ContactJing Yan

Zhejiang Hospital

zjicu@vip.163.com+86 133 3618 8688

Outcome results

None listed

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