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Impact of enteral ecoimmunonutrition on immunological response, nutritional status and tolerance to treatment in gastrointestinal malignancy patients receiving chemotherapy

Impact of enteral ecoimmunonutrition intervention on adjuvant chemotherapy and tolerance in patients with colorectal cancer

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400084224
Enrollment
Unknown
Registered
2024-05-13
Start date
2021-01-06
Completion date
Unknown
Last updated
2024-05-21

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

Conditions

gastrointestinal tumors

Interventions

the control group:In the control group, patients received essential health education (healthy diets and other precautions), and a regular diet (without the use of Ayunutri).
the enteral ecoimmunonutrition group:In the EIN group, besides regular diet, patients were administered orally a jar (237 mL) of Ayunutri from the first day of chemotherapy for 42 days.

Sponsors

Hebei General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: ? with a diagnosis of esophageal, gastric, or colorectal cancer confirmed by surgical/endoscopic pathology; ? the cancer was radiologically assessed as stage III or IV according to the American Joint Committee on Cancer (AJCC) staging manual (8th edition), along with the presence of assessable lesions; ? the patient could be fed orally; ? with an expected survival of =3 months; ?requiring systemic chemotherapy (biweekly or three-weekly combination chemotherapy regimens); and ? aged 18 - 80 years (including 18 and 80 years).

Exclusion criteria

Exclusion criteria: ?with co-existing hepatic and renal insufficiency and other metabolic diseases that could not be controlled by medications; ? with acute or chronic infections at other sites; ?use of steroids or immunosuppressive agents; ? with accompanying malignant tumors; ? with complete intestinal obstruction; ? could not be fed orally; and? allergic to the study drug or unable to complete the study due to other reasons.

Design outcomes

Primary

MeasureTime frame
assessment of the nutritional risk;assessment of the nutritional status;

Secondary

MeasureTime frame
assessment of the quality of life ;assessment of the chemotherapy toxicities;

Countries

China

Contacts

Public ContactJia Yitao

Hebei General Hospital

jiayitao99@163.com+86 859888367

Outcome results

None listed

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