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Clinical Observation Experiments on the Benefits of Recovery of Postoperative/Chemoradiotherapy Patients Taking QuanShiJinKe® Microproteins

Clinical Observation Experiments on the Benefits of Recovery of Postoperative/Chemoradiotherapy Patients Taking QuanShiJinKe® Microproteins

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500103406
Enrollment
Unknown
Registered
2025-05-28
Start date
2025-05-30
Completion date
Unknown
Last updated
2025-06-02

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

Conditions

The immunity of cancer patients decreases after chemotherapy

Interventions

QuanShiJinKe microproteins taking group:QuanShiJinKe microproteins

Sponsors

Affiliated Hospital of Jinggangshan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
10 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Select patients from the oncology department who have undergone surgery or are currently undergoing radiotherapy or chemotherapy, with an age requirement of 10 years or older and 75 years or younger; 2. Based on clinical history, symptoms, signs, and imaging data, the diagnosis is confirmed by pathology as a tumor; 3. The tumor patient has not received surgical treatment and is planned to undergo radiation therapy combined with synchronous therapy; 4. Weight loss, but less than 10%; 5. Decreased dietary intake, but greater than 60% of the target feeding amount; 6. PG-SGA (Patient Generated Subjective Global Assessment) score = 4 points; 7. Organ function is good, including sufficient bone marrow reserve function: absolute neutrophil (lobulated and banded) count (ANC) = 1.5 × 109/L, platelets = 100 X 109/L, and hemoglobin = 9g/dL. Liver: Bilirubin = 1.5 times normal E-limit (× ULN), alkaline phosphatase (AP), aspartate aminotransferase (ASll), and alanine aminotransferase (ALT) 1.5XULN. Kidney: Creatinine clearance rate (Ccr) calculated according to Cockcroft and Gault formulas is 980 mL/min. 8. Expected lifespan = 12 weeks; 9. Can understand the purpose and adverse reactions of the study, patients and their relatives have given informed consent to participate in this study and voluntarily signed informed consent forms.

Exclusion criteria

Exclusion criteria: 1. Severe malnutrition (weight loss>10% or serum albumin<30 g/L or BMI<18.5 kg/m2); 2. Serious heart, lung, and brain diseases, etc; 3. Combined with severe renal insufficiency; 4. Combined infection related fever; 5. The existence of uncontrollable diabetes or other metabolic diseases; 6. There is intestinal obstruction that prevents diet and enteral nutrition; 7. Patients who are known to be allergic or intolerant to any component of parenteral or enteral nutrition for research purposes; 8. Alcohol or drug addiction: pregnancy or breastfeeding; Or women of childbearing age refuse contraception; 9. Patients with severe brain metastases from tumors; 10. Obstructing the signing and understanding of informed consent by individuals; 11. Patients who, for any other reason, cannot complete this study as determined by the researchers.

Design outcomes

Primary

MeasureTime frame
Blood routine;Blood biochemistry;Immunity;Patient weight changes,;Non fat components,;Skeletal muscle changes,;

Secondary

MeasureTime frame
Body improvement after treatment;

Countries

China

Contacts

Public ContactShengping Long

Affiliated Hospital of Jinggangshan University

longssengping@163.com+86 158 7963 6861

Outcome results

None listed

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