ACTRN12619001779167尚未招募2 期
sing acamprosate to investigate a new target for treatment in Prader-Willi Syndrome
适应症
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
- 入组人数
- 30
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
- Non-randomised trial
- 主要目的
- Treatment
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 30 Years（—）
- 性别
- All
入选标准
- •1. Aged between 18 to 30 years.
- •2. For participants with PWS, a confirmed genetic diagnosis of PWS.
- •3. Provide voluntary, written informed consent (all participants). For participants with PWS, parent / legal guardian also provides voluntary, written consent.
排除标准
- •1.Aged 17 years or younger and 31 years or older.
- •2.MRI contraindications (e.g. pregnant, metal in the body, insulin pumps, vertigo, claustrophobia, etc)
- •3.For PWS participants, comorbid psychiatric or neurological disorder that is not associated with PWS
- •4.For controls, no known neurological, psychiatric, neurogenetic or serious medical condition
- •5.Currently receiving treatment with a GABA compound
- •6.For non-GABA compounds, concomitant drug use will be allowed as long as there has been stable dosing for at least 4 weeks prior to participation
- •7.If evidence of potential renal failure creatine levels will be measured and participants with a creatinine clearance < 30 mL/min will be excluded.
- •8.Known sulphite hypersensitivity
- •9.Pregnant or breastfeeding women
研究者
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