Skip to content

Lingzhi for Cancer Children

A Randomized, Double-Blind, Placebo-Controlled, Parallel Study of the Clinical Effects of Ganoderma Lucidum (Ling Zhi) in Children With Cancer

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00575926
Enrollment
58
Registered
2007-12-18
Start date
2002-09-30
Completion date
2007-09-30
Last updated
2007-12-18

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

Conditions

Pediatric Cancers

Keywords

Randomized controlled trial, Lingzhi, Immune functions, Quality of life, Survival

Brief summary

Ganoderma lucidum (Lingzhi) is a Traditional Chinese Medicine which is widely used as a means to 'strengthen immunity' among patients with cancers. However, there is no published randomized controlled clinical trial on its efficacy and safety despite the many in vitro studies on its anti-viral, anti-oxidative, anti-tumour, radioprotective, hepato-protective and immunomodulatory effects. This study was a randomized, double-blind, placebo-controlled, parallel clinical trial that investigated the benefits and safety of Ganoderma lucidum (Lingzhi) in treating children with cancers. Patients were randomized to receive identical capsules of either Lingzhi or placebo for six months. The primary outcome was the general Paediatric Quality of Life score. Secondary outcomes included immune functions, infection-related morbidities, complete blood counts and serum biochemistry, and overall and event-free survival.

Detailed description

Alternative and complementary medicine are widely used in treating children with cancers. A population-based survey in British Columbia revealed that they were used by 42% of the respondents. Among Chinese in Hong Kong, Traditional Chinese Medicine (TCM) is also widely practiced. Some 60% of the population had consulted TCM practitioners at one time or another. TCM use could be dated back to more than five thousand years ago, and written records were available for over two thousand years. TCM is considered to be an integral part of the Chinese culture. In our experience, TCM is believed to be commonly used to 'strengthen immunity and promote health' among local children with cancers, despite the lack of well-designed study to prove its usefulness. Ganoderma lucidum (Ling Zhi) is a mushroom long-used in China for a broad range of disorders. Its use is common in the general population and among both adults and children with a wide range of malignancies. However, there is no randomized controlled trial to support its clinical efficacy and safety. Therefore, we conducted this clinical trial of Ganoderma lucidum (Ling Zhi) among Hong Kong children with cancers.

Interventions

LingZhi or Placebo 300 mg x 4 or 300 mg x 6 capsules daily according to age group

Sponsors

Prince of Wales Hospital, Shatin, Hong Kong
CollaboratorOTHER
Queen Elizabeth Hospital, Hong Kong
CollaboratorOTHER
Princess Margaret Hospital, Hong Kong
CollaboratorOTHER_GOV
Chinese University of Hong Kong
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
2 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* Male and female patients aged 2-18 years * Acute lymphoblastic leukaemia who completed induction chemotherapy and pending maintenance chemotherapy treatment * Solid tumours completed chemotherapy * Aute myeloid leukaemia who completed induction and consolidation chemotherapy treatment * All patients and their parents signed informed written consent

Exclusion criteria

* Relapsed cancer patients * Received Traditional Chinese Medicine (TCM) treatment within preceding one month * Could not swallow capsules * Syndromal disorders (e.g. Down syndrome) * History of hypersensitivity reaction to Lingzhi or any TCM * Significant gastrointestinal, renal, hepatic, bronchopulmonary, neurological, cardiovascular or allergic diseases * In the judgement of investigators were unable to comply with study protocol requirements

Design outcomes

Primary

MeasureTime frame
Generic and cancer-specific Pediatric Quality-of-Life assessment1 year

Secondary

MeasureTime frame
Cellular immune functions; blood counts and biochemistry for patient safety; infection-related morbidities; overall and event-free survival1 year

Countries

Hong Kong

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026