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Comparison of the effects of home homogenates and formulated enteral nutrition on nutritional and functional status in ICU patients recovering from stroke surgery: a randomized, controlled clinical trial

Comparison of the effects of home homogenates and formulated enteral nutrition on nutritional and functional status in ICU patients recovering from stroke surgery: a randomized, controlled clinical trial

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400089101
Enrollment
Unknown
Registered
2024-09-02
Start date
2023-09-01
Completion date
Unknown
Last updated
2024-09-09

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

Conditions

ICU survivor of stroke

Interventions

Experimental group:Home homogenate preparation nutritional support + routine rehabilitation therapy
Control group:Receive nutritional support with formulated enteral nutrition and routine rehabilitation therapy, target energy: body weight (kg) × 30 (kcal/ day), intake of 1.2 g/kg of protein per day.

Sponsors

Shenzhen Second People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) ICU patients who survived initial ischemic stroke or hemorrhage stroke and recovered after surgery; (2) At least 18 years of age; (3) Onset time within 3 months; (4) The patient had tracheostomy status; (5) Intermittent feeding via nasal feeding tube; (6) NA-SF score less than 8; (7) Patients or family members agree to participate in the study and sign informed consent.

Exclusion criteria

Exclusion criteria: (1) progressive stroke patients; (2) Patients with BMI =28; (3) Fasting or associated with inflammatory gastrointestinal diseases; (4) There are patients with malignant tumors; (5) There are patients with hyperthyroidism; (6) There are patients with tuberculosis; (7) Patients with severe burn; (8) Participated in clinical trials of other drugs or medical devices during the same period.

Design outcomes

Primary

MeasureTime frame
Weight gain;

Secondary

MeasureTime frame
The MNA-SF score increases;The muscle circumference of the upper arm on the non-paralyzed side increased;Increased ability to perform activities of daily living Input only one outcomes name;

Countries

China

Contacts

Public ContactZhang Qiu

Shenzhen Second People's Hospital

zhangqiu1981@sina.com+86 158 9985 1549

Outcome results

None listed

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