ACTRN12610000121066终止3 期
Efficacy and safety of Ginkgo Biloba for cognitive function and fatigue in breast cancer patients after primary adjuvant treatment
适应症
试验速览
- 阶段
- 3 期
- 状态
- 终止
- 入组人数
- 72
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 o limit(—)
- 性别
- Female
入选标准
- •Diagnosis of invasive breast cancer for which definitive surgery was performed.
- •Patient has completed chemotherapy and/or radiotherapy and/or targeted therapy for adjuvant treatment (if received) for breast cancer at least six months previously. Patients who did not require chemotherapy are eligible but must be at least six months post surgery and radiotherapy.
- •Patient has completed at least 2 months of anti-cancer hormonal treatment (if received).
- •Patient is less than two years post completing primary adjuvant treatment.
- •Self report cognitive symptoms based on a Single Item Question assessing their subjective change in cognitive function since their cancer diagnosis. Participants must select one of three possible responses (yes, no, unknown) to the question: Do you think your brain is working as well as it was before your cancer diagnosis?” To meet eligibility, participants must choose the NO” response.
- •Speak fluent English and read to at least year 8 standard;
- •Written informed consent;
- •Accessible for treatment and follow-up
排除标准
- •Eastern Cooperative Oncology Group (ECOG) performance status < or = 2;
- •Any evidence of extra-nodal metastatic disease;
- •Any major pre-existing psychiatric history or dementia, alcohol abuse, current use of psychotropic medication that might lead to cognitive problems other than benzodiazepines for nausea or sleep or selective serotonin reuptake inhibitor (SSRI) for hot flashes;
- •Pre-existing neurological condition or any other co-morbidity which may interfere with their ability to perform cognitive testing;
- •Previous chemotherapy for a malignancy.
- •Life expectancy < 2years;
- •use of Ginkgo biloba within 4 weeks of randomisation;
- •Any contraindication to taking ginkgo biloba.
研究者
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