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The use of Ganoderma for supportive care of patients undergoing palliative cancer care- A randomized controlled clinical trail

The use of Ganoderma for supportive care of patients undergoing palliative cancer care- A randomized controlled clinical trail

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500101760
Enrollment
Unknown
Registered
2025-04-29
Start date
2024-08-01
Completion date
Unknown
Last updated
2025-05-05

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

Conditions

Tumor

Interventions

Ganoderma lucidum spore powder + enteral nutrition powder group:Ganoderma lucidum spore powder
Enteral nutrition powder group:Enteral nutrition powder

Sponsors

The University of Hong Kong-Shenzhen Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1: All cases are subject to pathology and or cytology for a diagnosis of malignant tumorpathological type is not restricted; 2: Aged 18 years or above; 3: Expected survival time longer than 6 months; 4: Undergoing palliative care; 5: Have a functional digestive tract.

Exclusion criteria

Exclusion criteria: 1: Disseminated intravascular coagulation or severe thrombocytopenia with a bleeding tendency ie low platelet count 35000L INR 15 hemoglobin90 gdL; 2: Inability to swallow medicinal capsules; 3: Non-functional digestive tract (tumor compression, gastrointestinal obstruction); 4: Patients with gastrointestinal tumors; 5: Inability to read and understand Chinese; 6: Severe cognitive impairment(SLUMS <=20); 7: Not given written informed consent; 8: Allergy to ganoderma lucidum spore powder, milk or soy protein is known; 9: Galactosemia.

Design outcomes

Primary

MeasureTime frame
quality of life;

Secondary

MeasureTime frame
Cancer related symptoms;

Countries

China

Contacts

Public ContactFengming Kong

The University of Hong Kong-Shenzhen Hospital

Kong0001@hku.HK+86 189 2523 2792

Outcome results

None listed

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