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Nutrition Intervention is Beneficial in Changes the Prognosis of Loco-Regionally Advanced Nasopharyngeal Carcinoma Patients for the Worse

Nutrition Intervention is Beneficial in Changes the Prognosis of Loco-Regionally Advanced Nasopharyngeal Carcinoma Patients for the Worse

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000029399
Enrollment
Unknown
Registered
2020-01-29
Start date
2020-01-28
Completion date
Unknown
Last updated
2020-02-03

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

Conditions

Nasopharyngeal Carcinoma

Interventions

experimental group:individualized, regular and intensive nutrition
control group:general advice and nutrition booklet

Sponsors

Guigang City People's Hospital, The Eighth Affiliated Hospital of Guangxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
17 Years to 77 Years

Inclusion criteria

Inclusion criteria: 1. Aged 17 ~ 77 years; pathological diagnosis of WHO type II ~ III nasopharyngeal carcinoma; 2. The clinical stage is stage III ~ IVA; patients with nasopharyngeal carcinoma who need concurrent chemoradiotherapy; 3. Expected survival time is at least 6 months; 4. KPS score is greater than or equal to 70; 5. Sign the informed consent; 6. No history of severe heart disease and coronary heart disease; 7. Leukocyte count is greater than or equal to 4.0 x 10^9 / L, absolute neutrophil count is greater than or equal to 2.0 x 10^9 / L, platelet count is greater than or equal to 100 x 10^9 / L, and hemoglobin is greater than or equal to 80 g / L; 8. Total bilirubin, alanine aminotransferase and aspartate aminotransferase are all less than or equal to the upper limit; 9. Urine creatinine is less than or equal to the upper limit of normal value and creatinine clearance is 60 mL / min or more.

Exclusion criteria

Exclusion criteria: 1. Have a history of other malignant tumors; 2. Pregnant or lactating women; 3. Concomitant diseases or conditions affect the safety of patients during normal enrollment and study; 4. Existing active mental disorders or other mental illnesses that affect patients' signed informed consent and understanding; 5. Have severe active infections (including hepatitis); 6. Those who are allergic or sensitive to the test sample; 7. Patients with diabetes; 8. Investigators consider patients with poor compliance.

Design outcomes

Primary

MeasureTime frame
Progression free survival;

Secondary

MeasureTime frame
Overall survival;Relapse-free survival;

Countries

China

Contacts

Public ContactHaizhen Yi

Department of Oncology, Guigang City People's Hospital, the Eighth Affiliated Hospital of Guangxi Medical University

yhz228815@163.com+86 15807851995

Outcome results

None listed

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