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The Impact of Oral Nutritional Supplements for Food for Special Medical Purposes (ONS-FSMP), Specifically Tumor-Specific Complete Nutrition Formulas, on Chemotherapy Completion Rate, Non-Anticancer Treatment Costs, and Adverse Events in Patients with Solid Tumors Receiving Chemotherapy: A Prospective Real-World Study

The Impact of Oral Nutritional Supplements for Food for Special Medical Purposes (ONS-FSMP), Specifically Tumor-Specific Complete Nutrition Formulas, on Chemotherapy Completion Rate, Non-Anticancer Treatment Costs, and Adverse Events in Patients with Solid Tumors Receiving Chemotherapy: A Prospective Real-World Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500107919
Enrollment
Unknown
Registered
2025-08-21
Start date
2025-08-31
Completion date
Unknown
Last updated
2025-08-25

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

Conditions

Cancer

Interventions

Oral Food for Special Medical Purposes Group (Tumor-Specific Complete Nutrition Formulas):None
Control group:None

Sponsors

Yunnan Provincial Tumor Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Only patients who meet all the following enrollment criteria can be included in this study: 1) Aged 18-80 years, regardless of gender; 2) Patients with solid tumors scheduled to receive at least 4 cycles of chemotherapy, and those planned to receive combined with other systemic anti-tumor therapies are allowed to enroll; 3) Patients assessed as having malnutrition or at risk of malnutrition (score >=3) by nutritionists using the Nutritional Risk Screening 2002 (NRS2002); 4) Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) score of 0-2; 5) Voluntarily sign the informed consent form.

Exclusion criteria

Exclusion criteria: Patients with any of the following conditions will be excluded from this study: 1) Concurrent multiple primary tumors; 2) Having taken nutritional supplements or drugs containing immunomodulatory formulas (with an average daily intake of DHA + EPA = 500 mg/d, or containing arginine or glutamine) within 1 month; 3) Patients with complicated active infections (such as sepsis) or severe diseases such as cognitive impairment caused by neurological or mental diseases, severe hematological diseases, severe digestive tract diseases, etc.; 4) Pregnant or lactating women; 5) Patients who cannot receive treatment on time, cannot cooperate with follow-up, or have difficulty taking oral nutritional formulas; 6) Patients known to be allergic to the active ingredients of the total nutritional formula food for special medical purposes in oncology, or patients judged by researchers to be unsuitable for using Suyisu; 7) Patients participating in other clinical trials.

Design outcomes

Primary

MeasureTime frame
Chemotherapy Completion Rate;

Secondary

MeasureTime frame
Non-Antineoplastic Medical Costs;Patient Out-of-Pocket Payment;Weight Change Percentage;Chemotherapy Dose Reduction Rate;Quality of Life;Treatment-Related AEs;Medical insurance covers non-anti-tumor treatment expenses;Total Treatment Cost;Chemotherapy Delay Rate;Weight Change;Adverse Events;Standard-Dose Chemotherapy Completion Rate;

Countries

China

Contacts

Public ContactLi Gaofeng

Yunnan Provincial Tumor Hospital

ligaofenghl@126.com+86 139 8712 3539

Outcome results

None listed

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