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临床试验/NCT04905446
NCT04905446已完成不适用

Measurement of NAD+ Synthesis in Human Skeletal Muscle

AdventHealth Translational Research Institute1 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2021年9月10日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
15
试验地点
1
主要终点
Measurement of NAD+ mass isotopomers in extracts from human muscle and skin tissue biopsies as determined by liquid chromatography-mass spectrometry (LC-MS)

研究概览

简要总结

The key objective of this pilot research study is to dose human volunteers with a heavy (non-radioactive) isotope derivative of nicotinamide to detect NAD synthesis in human skeletal muscle. The ultimate goal is to examine the impact of lifestyle choices, aging, nutraceuticals, and drugs on the rate of NAD synthesis in human subjects.

研究设计

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

入排标准

年龄范围
21 Years 至 40 Years(Adult)
性别
Male
接受健康志愿者
是

入选标准

  • •Healthy male subjects who, at the time of screening are between the ages of 21 to 40 years of age, inclusive.
  • •BMI between 20-30 kg/m2 at the screening visit (SV)
  • •Understands the procedures and agrees to participate by giving written informed consent
  • •Willing and able to comply with the scheduled study day and other study procedures

排除标准

  • •Acute or chronic medical conditions or medication that would contraindicate the participation in the research testing or could potentially affect metabolic function including, but not limited to:
  • •History of type 1 or type 2 diabetes mellitus, including pre-diabetes (HbA1c > 5.7)
  • •History of any antihyperglycemic agent (e.g., insulin)
  • •Currently taking medications that can alter glucose homeostasis (e.g., steroids, glucocorticoids, nicotinic acid) or skeletal muscle metabolism
  • •History of taking Tru Niagen, Basis (or any other NR-containing NAD+ booster) or niacin supplements.
  • •Any bleeding disorders
  • •Currently taking any aspirin (ASA) (including baby ASA) or NSAIDs (ibuprofen, naproxen, etc.) that cannot be safely stopped throughout the study. There is a recommended hold on NSAIDs and/or ASA for at least 2 days prior to biopsy, although not exclusionary
  • •Presence of bruising in lower extremities
  • •Any major surgery within the past 3 months
  • •Any acute or chronic infections
  • •Evidence or history of clinically significant hematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric, neurological or allergic diseases, but excluding untreated, asymptomatic, seasonal allergies at the time of intervention.
  • •Previous difficulty with lidocaine or other local anesthetic agents
  • •Thyroid dysfunction (suppressed TSH, elevated TSH <10 µIU/ml if symptomatic or elevated TSH >10 µIU/ml if asymptomatic)
  • •Uncontrolled hypertension (BP >160 mmHg systolic or >100 mmHg diastolic)
  • •Use of tobacco or nicotine-containing products within the last 12 months.
  • •Chronic kidney disease with GFR of < 60
  • •Anemia (hemoglobin <12 g/dl) during screening
  • •History of human immunodeficiency virus (HIV), hepatitis B or hepatitis C
  • •Liver function testing for ALT or AST greater than or equal to 2 times the upper limit of normal
  • •Participation in studies involving investigational drug(s) within 30 days prior to Screening visit
  • •Blood donation (excluding plasma donations) of approximately 1 pint (500 mL) or more within 56 days prior to Screening (participants may not donate blood any time during the study, through the final study day)
  • •Presence of any condition that, in the opinion of the Investigator, compromises participant safety or data integrity or the participant's ability to complete study days Labs may be repeated at the discretion of the PI, MI or Sub-investigators (Sub-I).

研究组 & 干预措施

Healthy male subjects

Other

干预措施: Deuterated nicotinamide (D4-NAM) IV infusion (Other)

Healthy male subjects

Other

干预措施: Skeletal muscle biopsy (Procedure)

Healthy male subjects

Other

干预措施: Skin tissue biopsy (Procedure)

结局指标

主要结局

Measurement of NAD+ mass isotopomers in extracts from human muscle and skin tissue biopsies as determined by liquid chromatography-mass spectrometry (LC-MS)

时间窗: 4 weeks

次要结局

未报告次要终点

研究者

发起方
AdventHealth Translational Research Institute
申办方类型
Other
责任方
Sponsor

研究点 (1)

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