ACTRN12623001042639招募中1 期
Efficacy of Low Dose Naltrexone for the treatment of symptoms of Post COVID-19 Condition
适应症
试验速览
- 阶段
- 1 期
- 状态
- 招募中
- 入组人数
- 56
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 65 Years(—)
- 性别
- All
入选标准
- •Participants with long COVID according to the World Health Organization working case definition (Individuals with a history of probable or confirmed SARS-CoV-2 (COVID-19) three months from COVID-19 onset with symptoms lasting at least two months).
- •Present with symptoms including cognitive disturbances (brain fog), sleep disturbances, and/or body pain.
排除标准
- •i.Current respiratory infections
- •ii.Intercurrent SARS-CoV-2 reinfection during trial period (this will be considered drop-out)
- •iii.Previous clinical diagnosis of ME/CFS
- •iv.Chronic pain history prior to long COVID onset
- •v.Adverse reaction to LDN or compounded constituents
- •vi.Chronic opioid or substitution therapy
- •vii.Daily opioid use in three months prior to, or during trial
- •viii.Substance abuse, dependence, addiction
- •ix.History of drug, alcohol abuse and recreational drugs
- •x.Pregnancy or breastfeeding
- •xi.Renal dysfunction (eGFR greater than 30 ml/min/1.73m2), liver dysfunction (ALT or AST greater than 300 IU/L).
- •xii.Active cancer.
- •xiii.Inflammatory (rheumatological, GIT, dermatological) or neurological condition (demyelinating).
- •xiv.Neuroimmune modulators: DMARDs, steroids, minocycline, metformin.
- •xv.History of anxiety, depression and/or other psychiatric concerns.
- •xvi.Language, cognition, no computer literacy.
研究者
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