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临床试验/DRKS00023348
DRKS00023348已完成4 期

Acupuncture in chemotherapy-induced dysgeusia – a randomized controlled trial – AcuDysg - AcuDysg

Institut für komplementäre und integrative Medizin UniversitätsSpital Zürich0 个研究点目标入组 22 人开始时间: 2020年11月3日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
22

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
Randomized controlled study
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 one(—)
性别
All

入选标准

  • indication of supportive routine care acupuncture treatment for fatigue, with a fatigue intensity of at least 3 on a numeric rating scale (NRS 1-10)
  • - dysgeusia of at least 5 on NRS (=moderate dysgeusia, NRS 1-10) in the screening tool (adapted from Zabernigg A. et al., 2010)
  • - actually treated with a chemotherapy regime that includes taxanes, platinum-based antineoplastic drugs or antrazyclins
  • - chemotherapy treatment is planned to continue at least 8 weeks after beginning of acupuncture treatment
  • - breast, ovarian, endometrial, pancreas, colorectal, lung, prostate cancer, urothelial carcinoma, germ cell tumor or sarcoma
  • - lymphomas with bone marrow infiltration <50% that are under treatment with antrazyclins
  • - performance status of ECOG 0-1
  • - can eat normal food without pain or swallowing problems
  • - internet access and interested to use e-learning

排除标准

  • - currently receive acupuncture treatment
  • - dysgeusia that occurred independently of the chemotherapy treatments of the current cancer
  • - confirmed positive COVID-19 test with associated dysgeusia prior to chemotherapy treatment
  • - increased risk of bleeding e.g. caused by haemophilia or platelets<50000 µl
  • - coexisting MDS
  • - don’t speak sufficient German
  • - mucositis and dysgeusia with an impact on nutrition (pain or swallowing problems)
  • - currently receiving or have a planned radiotherapy during the intervention period (within the next 12 weeks) in the head/neck area

研究者

发起方
Institut für komplementäre und integrative Medizin UniversitätsSpital Zürich

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