ISRCTN72727460已完成不适用
European trial of Minocycline IN Amyotrophic Lateral Sclerosis
King's College London (UK)0 个研究点目标入组 1,000 人开始时间: 2007年5月3日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 1,000
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •1. Possible, probable (clinically or laboratory) or definite ALS according to the revised version of the El Escorial World Federation of Neurology criteria (The ?Airlie House Statement?: http://www.wfnals.org/). The onset form (bulbar or limb) and disease type (familial or sporadic) will be recorded; source documents will include a full report of an electromyogram (EMG) reported by an experienced neurophysiologist as compatible with ALS
- •2. Disease duration more than 6 months (required by the El Escorial Criteria as the minimum time required to determine that there has been progression) and less than 5 years (inclusive); disease onset defined as date of first muscle weakness
- •3. Vital Capacity (VC) greater than or equal to 40 % of predicted
- •4. Age: greater than or equal to 18 years (inclusive)
- •5. Sex: male or female. In the case of a female with childbearing potential, the patient must use adequate contraceptive measures and must not be pregnant or breast-feeding
- •6. Continuously treated with riluzole for at least 3 months and stabilised at 100 mg/day (50 mg twice a day) without significant adverse drug reactions
- •7. Capable of understanding the information given and giving fully informed consent
排除标准
- •1. Previous participation in another clinical study within the preceding 12 weeks
- •2. Tracheostomy, assisted ventilation of any type during the preceding three months
- •3. Existing gastrostomy
- •4. Any medical condition known to have an association with motor neuron dysfunction which might confound or obscure the diagnosis of ALS
- •5. Presence of any concomitant life-threatening disease or any disease or impairment likely to interfere with functional assessment
- •6. Confirmed hepatic insufficiency or abnormal liver function (aspartate aminotransferase [AST] and/or alanine aminotransferase [ALT] greater than 1.5 the upper limit of the normal range)
- •7. Renal insufficiency (serum creatinine greater than 200 µmol/L [2.26 mg/dL])
- •8. Evidence of major psychiatric disorder or clinically evident dementia precluding evaluation of symptoms
- •9. Known hypersensitivity to any component of the study drugs or to drugs in this class
- •10. Likely to be unco-operative or to fail to comply with the trial requirements or to be inaccessible in the event of an emergency
- •11. Unable or unwilling to use an effective method of contraception if a woman of childbearing age
- •We have chosen inclusion criteria that are permissive (i.e., sensitive) without sacrificing specificity. The El Escorial Criteria of the World Federation of Neurology (The ?Airlie House Statement?: http://www.wfnals.org/) are internationally accepted research diagnostic criteria with high specificity and sensitivity.
研究者
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