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临床试验/ACTRN12623001042639
ACTRN12623001042639招募中1 期

Efficacy of Low Dose Naltrexone for the treatment of symptoms of Post COVID-19 Condition

Griffith University0 个研究点目标入组 56 人开始时间: 2023年9月26日最近更新:
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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