EUCTR2019-000702-30-DK进行中(未招募)1 期
Fibromyalgia and Naltrexone: The FINAL study - FINA
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 入组人数
- 99
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- Female
入选标准
- •-Women aged 18-64 years
- •-Understands and writes Danish
- •-Fulfills the ACR1990 criteria for fibromyalgia
- •-A minimum score of 4 in self-reported average pain during the last 7 days on a 0-10 NRS at baseline
- •-All fertile women have to use safe anti conception
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 100
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range 0
排除标准
- •-Known allergy against naltrexonehydroclorid
- •-Pregnancy or breastfeeding. A negative pregnancy test has to be available for all fertile subjects at baseline
- •-Use of opioids or NSAIDs up to 4 weeks before inclusion in the trial
- •-Abuse of alcohol or other substances
- •-Inflammatory rheumatic diseases
- •-Demyelinating diseases
- •-Active cancer
- •-Liver dysfunction (ALAT must not be elevated more than 2-fold over highest reference level)
- •-Kidney dysfunction (GFR < 59 mL/min)
- •-Psychotic diseases
- •-History of suicide attempts
- •-Suicide ideation – evaluated using PHQ-9 (Item 9 has to be answered never”)
研究者
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