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临床试验/NCT01252979
NCT01252979已完成早期 1 期

Ketones & Mitochondrial Heteroplasmy

The University of Texas Health Science Center, Houston2 个研究点 分布在 1 个国家目标入组 13 人开始时间: 2010年12月1日最近更新:
适应症

试验速览

阶段
早期 1 期
状态
已完成
入组人数
13
试验地点
2
主要终点
Heteroplasmy

研究概览

简要总结

The current study is a prospective evaluation of the ability of ketosis to shift mitochondrial DNA (mtDNA) heteroplasmy in subjects harboring a known mutation in their mtDNA at position 3243 (A>G). Subjects will be given supplemental medium chain triglycerides (MCTs) for a period of 6 months. mtDNA heteroplasmy will be measured 3 months prior to treatment, at treatment initiation, and 6 months after initiation.

The primary objective of the current study is to determine if there is a shift in heteroplasmy in patients harboring the 3243 A>G mtDNA mutation to a more favorable (higher wild-type) profile while in a state of ketosis.

详细描述

The current study is a prospective evaluation of the ability of ketosis to shift mitochondrial DNA (mtDNA) heteroplasmy in subjects harboring a known pathogenic mutation in their mtDNA at position 3243 (A>G). Subjects will be induced in to ketosis by administration of supplemental medium chain triglycerides (MCTs) for a period of 6 months. mtDNA heteroplasmy will be assessed 3 months prior to treatment, at treatment initiation, and 6 months after initiation.

The primary objective of the current study is to determine if there is a shift in heteroplasmy in patients harboring the 3243 A>G mtDNA mutation to a more favorable (higher wild-type) genotypic profile while in a state of ketosis.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

性别
All
接受健康志愿者

入选标准

  • Subject is informed and given ample opportunity to consider his/her participation and has given his/her written consent.
  • Subject is willing and able to comply with all trial requirements.
  • Subject harbors the 3243 A>G mtDNA mutation at a level detectable in blood.
  • Female subjects of child-bearing potential must not be pregnant. Female subjects of child-bearing potential (not surgically sterile or 2 years post-menopausal) must also agree to use appropriate contraceptive methods (abstinence, oral, injectable, implantable, or barrier) for the duration of the trial.
  • Subject must not have diabetes mellitus.

排除标准

  • Subject is currently participating or has participated within the last 2 months in any clinical trial involving treatment of mitochondrial disorders with MCT supplementation or induction of ketosis.
  • Subject has a medical condition that could reasonably be exacerbated by ketone supplementation (including diabetes mellitus).
  • Subject is unable to give reasonable informed consent/assent.
  • Subject is a pregnant or nursing female.

结局指标

主要结局

Heteroplasmy

时间窗: 9 months

Blood samples will be used to measure the degree of mitochondrial DNA heteroplasmy

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Mary Kay Koenig

Principle Investigator

The University of Texas Health Science Center, Houston

研究点 (2)

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