Pediatric Cancers Clinical Trial
Official title:
A Randomized, Double-Blind, Placebo-Controlled, Parallel Study of the Clinical Effects of Ganoderma Lucidum (Ling Zhi) in Children With Cancer
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.
Status | Completed |
Enrollment | 58 |
Est. completion date | September 2007 |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 2 Years to 18 Years |
Eligibility |
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 |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Hong Kong | Department of Pediatrics and Adolescent Medicine, Princess Margaret Hospital | Hong Kong | |
Hong Kong | Department of Pediatrics, Queen Elizabeth Hospital | Hong Kong | |
Hong Kong | Department of Pediatrics, The Chinese University of Hong Kong | Hong Kong |
Lead Sponsor | Collaborator |
---|---|
Chinese University of Hong Kong | Prince of Wales Hospital, Shatin, Hong Kong, Princess Margaret Hospital, Hong Kong, Queen Elizabeth Hospital, Hong Kong |
Hong Kong,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Generic and cancer-specific Pediatric Quality-of-Life assessment | 1 year | No | |
Secondary | Cellular immune functions; blood counts and biochemistry for patient safety; infection-related morbidities; overall and event-free survival | 1 year | Yes |
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