Construction and empirical study of enteral and parenteral nutrition management plan for patients with sepsis based on evidence-based evidence

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2600125459

Enrollment

Unknown

Registered

2026-05-27

Start date

2026-06-01

Completion date

Unknown

Last updated

2026-06-01

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

Conditions

Sepsis

Interventions

Control group:Routine nutritional care

Intervention group:Evidence-based enteral and parenteral nutrition management program for sepsis patients + routine care

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >= 18 years old; 2. Comply with the diagnostic criteria of the International Consensus on the Definition of Sepsis and Septic Shock (Sepsis-3); 3. The duration of stay in the intensive care unit (ICU) is >= 24 hours; 4. It is expected that enteral nutrition (EN) and/or parenteral nutrition (PN) support will be required; 5. The patient or their legal representative signs a written informed consent form (if the patient is unable to sign it); 6. The patient was initially diagnosed with sepsis and had not received systematic nutritional intervention before this admission.

Exclusion criteria

Exclusion criteria: 1. Pregnant or lactating women; 2. Combined with severe liver and kidney failure (such as Child-Pugh grade C, eGFR < 15 mL/min/1.73m^2); 3. There is intestinal dysfunction or intestinal obstruction, making it impossible to implement enteral nutrition; 4. The expected survival time is less than 72 hours or the patient is in the terminal stage of the disease; 5. Currently participating in other interventional clinical studies or nutrition-related trials; 6. History of immune deficiency (such as HIV infection, long-term use of immunosuppressants); 7. There is a history of allergy or severe intolerance to conventional nutritional preparations; 8. Incomplete clinical data or inability to cooperate in the collection of research data.

Design outcomes

Primary

Measure	Time frame
Triceps skinfold thickness;Body massindex BMI;Nutritional indicators for patients with sepsis: albumin, preprotein, hemoglobin, total serum protein level, transferrin;	—

Secondary

Measure	Time frame
Clinical nurse nutrition nursing ability;Incidence of complications;	—

Countries

China

Contacts

Public ContactZhu Shoujun

The First Affiliated Hospital of University of Science and Technology of China (Anhui Provincial Hospital)

7802301@qq.com+86 551 62282871

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026