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临床试验/NCT02333305
NCT02333305已完成3 期

Evolution of Albumin on AOA1 Patients Supplemented With Coenzyme Q10

Assistance Publique - Hôpitaux de Paris1 个研究点 分布在 1 个国家目标入组 19 人开始时间: 2013年6月1日最近更新:
适应症
干预措施

试验速览

阶段
3 期
状态
已完成
入组人数
19
试验地点
1
主要终点
Albuminemia

研究概览

简要总结

We propose a study on Ataxia with oculomotor apraxia type 1 (AOA1) in which Coenzyme Q10 (CoQ10) deficit has been observed. Main objectives of the study are :

  • To monitor evolution of albumin in patients affected with AOA1 while supplemented with CoQ10 ;
  • To measure with clinical scales and biological markers efficacy of supplementation on disease evolution.

AOA1 is characterised by Hypoalbuminemia. Disease duration is negatively correlated with albumin level. This study aims to understand mechanisms of the disease and our hypothesis is that correction or stabilization of albumin level with CoQ10 supplementation could impact disease evolution. The study is planned from 1 to 2 years supplementation. The CoQ10 is classified as a food supplement and has already been tested in other neurological conditions.

详细描述

Ataxia with ocular apraxia type 1 (AOA1) is an autosomal recessive cerebellar ataxia. Patients' phenotype associates early onset cerebellar ataxia, oculomotor apraxia, neuropathy and often intellectual disability, hypoalbuminaemia and hypercholesterolemia.

APTX gene mutations responsible for AOA1 disease were identified in a family previously reported with ataxia and Coenzyme Q10 deficiency. Therefore we measured muscle Coenzyme Q10 in six patients AOA1 and found decreased levels in five. Hypercholesterolaemia and low albumin levels represent hallmarks of the disease.

We thus propose therapeutic trial with Coenzyme Q10 in AOA1 patients, by using albumin evolution as primary endpoint.

Moreover several secondary endpoints will be performed:

  • clinical examination (SARA scale)
  • quantitative assessments of the ataxia (with the calculation of the Composite Cerebellar Functional Severity CCFS)
  • biological criteria (prealbumin, cholesterol, alphafoetoprotein, blood count, hepatic checkup)
  • oculographic examination.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

盲法说明

placebo

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •1. Diagnosis of ataxia with oculomotor apraxia type I (AOA1) confirmed by genetic molecular analysis
  • •2. Age ≥ 18 years
  • •3. Hypoalbuminemia
  • •4. Efficient contraception for women of childbearing potential (with pregnancy test during each visit)
  • •5. Signature of the written informed consent form
  • •6. Presence of a support person (for patient with cognitive disorders)

排除标准

  • •1. Hypersensitivity to one of the excipients (glycerin, ethanol, lecithin)
  • •2. Absence of hypoalbuminemia
  • •3. During the 2 months before inclusion :
  • •Use of CoQ10
  • •Treatment with antioxidants (vitamin C) and statins
  • •Use of drugs affecting mitochondrial activity
  • •Anti-cholesterol, thyroid hormones, anti-arrhythmic compounds, warfarin, metformin or clozapine
  • •4. Treatment with vitamin E, calcium, magnesium and/or other vitamins with a concentration superior to 149 UI during more than 3 months before inclusion
  • •5. Use of drugs interfering with catacholamine metabolism (reserpine, amphetamine, or inhibitors of the monoamine oxidase A, methylphenidate, cinnarizine) during the month before inclusion
  • •6. Non balanced treatment with anxiolytics, hypnotics, tranquillizers and/or antidepressants during the month before inclusion
  • •7. Hypothyroidism with thyroxin use
  • •8. Epilepsy
  • •9. Psychotic disorders
  • •10. Pregnancy or lactation period
  • •11. Woman of childbearing potential without efficient contraception
  • •12. Participant to other therapeutic studies during the month before inclusion
  • •13. Inability to receive a clear information on the research
  • •14. Inability to participate to the totality of the study
  • •15. Non affiliation to social security (beneficiary or assignee)
  • •16. Refusal of signing the consent form

研究组 & 干预措施

2

Placebo Comparator

Placebo of CoQ10 is a translucent nano-emulsion of well characterized nano particles. Lecithin (and) Alcohol (and) Glycerin (and) Aqua

干预措施: Sanomit Placebo (Other)

1

Experimental

Coenzyme Q10 (CoQ10) - is a Dietary complement that contains Coenzyme Q10 (Ubidecarenone) well characterized nano particles.

干预措施: CoQ10 (Dietary Supplement)

结局指标

主要结局

Albuminemia

时间窗: 2 years

Evolution of albuminemia every 6 months during 2 years.

次要结局

  • SARA scale(2 years)
  • prealbuminemia(2 years)
  • alfa-foeto-protein(2 years.)
  • Oculomotor evaluation(2 years)
  • EQ5D - PHQ9(2 years)
  • CCFS(2 years)
  • cholesterol(2 years.)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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