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A Randomized, Double-Blind, Parallel, Placebo-Controlled Study on the Evaluation of the Effect of Snow Lotus Stem Cell Small Molecule Peptides on the Nutritional Status of Cancer Patients?

A Randomized, Double-Blind, Parallel, Placebo-Controlled Study on the Evaluation of the Effect of Snow Lotus Stem Cell Small Molecule Peptides on the Nutritional Status of Cancer Patients?

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500102040
Enrollment
Unknown
Registered
2025-05-07
Start date
2025-04-03
Completion date
Unknown
Last updated
2025-05-12

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

Conditions

stomach cancer/esophageal cancer/lung cancer?

Interventions

test group 1(Gastric/esophageal cancer patients):Oral administration of Snow Lotus Stem Cell Small Molecule Peptides
test group 2(Lung cancer patients):Oral administration of Snow Lotus Stem Cell Small Molecule Peptides
placebo group(10 patients with Gastric/esophageal cancer patients , 10 patients with Lung cancer patient):placebo

Sponsors

Hefei Cancer Hospital,Chinese Academy of Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) Aged 18 years or older, regardless of gender; (2) Patients with lung cancer and gastric/esophageal cancer confirmed cytologically or histologically; (3) TNM stage II–IV; (4) Karnofsky Performance Status (KPS) score>=60; (5) Able to eat normally orally, with good adherence to nutritional therapy concepts and medical care; (6) Regularly receiving non-surgical treatments (e.g., chemotherapy, radiotherapy, immunotherapy) with an expected survival period of more than 6 months; (7) Presence of malnutrition or risk of malnutrition, with a PG-SGA score >=4; (8) Both patients and their families fully understand the potential benefits and risks of the study and have signed the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Combined severe cardiac, hepatic, or renal dysfunction; severe gastrointestinal diseases; uncontrolled chronic systemic diseases (e.g., diabetes, hypertension)?; (2) Concurrent use of other nutritional preparations that may interfere with trial outcomes?; (3) Contraindications to enteral or parenteral nutritional support?; (4) Pregnancy, lactation, or female patients of childbearing potential with positive baseline pregnancy tests?; (5) Allergy to soy products or severe allergic predisposition?; (6) Participation in other interventional clinical trials (including drugs, nutritional preparations, medical devices) within 4 weeks prior to screening?; (7) Investigator-determined unsuitability for study participation?.

Design outcomes

Primary

MeasureTime frame
Body Composition Analysis;Patient-Generated Subjective Global Assessment (PG-SGA) Score;Short Form Health Survey (SF-36) score;

Secondary

MeasureTime frame
Complete Blood Count (CBC);

Countries

China

Contacts

Public ContactWang Jinyun

Hefei Cancer Hospital,Chinese Academy of Sciences

2674028657@qq.com+86 551 6559 5111

Outcome results

None listed

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