ISRCTN60931429已完成未知
Clinical trial of the effect of oral administration of magnesium threoninate (L-TAMS) in morphine analgesia and tolerance
Xinhua Hospital (affiliated with Shanghai Jiaotong University School of Medicine)0 个研究点目标入组 116 人开始时间: 2018年1月24日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 116
研究概览
简要总结
2023 Results article in https://pubmed.ncbi.nlm.nih.gov/36703238/ (added 14/02/2024)
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1. Subjects voluntarily signed the informed consent
- •2. Patients suffering from cancer pain with treatment of morphine, aged from 18 to 80 regardless of gender
- •3. Survival time is expected to exceed 3 months
- •4. Moderate to severe pain, VAS >4 points or more, or outbreak of pain >3 times/day
- •5. Patients can follow the drug dose and follow-up plan
- •6. Patients can describe the symptoms, no serious infection, respiratory insufficiency and has the ability to cooperate
- •7. Non-allergic persons
- •8. No drug abuse or drug addiction
- •9. Non-lactating, pregnant women. Subjects who did not have a pregnancy plan within 1 month after the test
- •10. Patients did not participate in a drug test within 3 months before this test (including the test drug)
排除标准
- •1. Researchers think that there is any reason they can't be included
- •2. In poor situation, severe systemic infection or respiratory dysfunction and uncooperative
- •3. Suffering from severe respiratory system, cardiovascular system diseases, liver and kidney dysfunction, cancer
- •4. Patients who are allergic to magnesium threonate (L-TAMS)
- •5. Patient who has a history of drug abuse
- •6. Breastfeeding, gestational women or subjects who do not have a pregnancy plan within 1 month after the test
- •7. Patients who participated in a drug trial within 3 months before this trial
- •8. Patients does not meet the inclusion criteria
研究者
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