ISRCTN21659064已完成不适用
Comparison of the effects of intermittent boluses to simple continuous infusion on patient global perceived effect in intrathecal therapy for pain
South Tees Hospitals NHS Trust (UK)0 个研究点目标入组 34 人开始时间: 2012年7月30日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 34
研究概览
简要总结
- 2017 results in https://www.ncbi.nlm.nih.gov/pubmed/27651513 (added 22/01/2019)
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1. Are implanted with a programmable Intrathecal Therapy Drug Device (ITDD)
- •2. Have achieved stable pain relief on continuous flow
- •3. Are capable of giving informed consent
- •4. Are willing to sign the Informed Consent form
- •5. Are male or female
- •6. Aged between 18 years and 65 years of age
排除标准
- •1. Fail to give informed consent
- •2. Are incapable of answering the questionnaires: PGIC, EQ5D, VAS Score for physical or psychological reasons 3. Have non-Programmable Device ITDD
- •4. Have Patient Therapy Manager devices (PTM's)
- •5. Are using Ziconotide Intrathecal Therapy
- •6. Are programmed with bolus doses (flex doses)
- •7. Have severe limitation in function and mobility
- •8. Are pregnant or lactating
- •9. Are not practising a safe method of birth control
研究者
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