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临床试验/CTRI/2024/03/063457
CTRI/2024/03/063457已完成不适用

A double blind, randomized, single dose, three treatment, three way crossover, oral bioavailability study of investigational product containing β- analine in healthy, adult, human participants under fasting conditions.

Natural Alternatives International1 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2024年3月5日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
12
试验地点
1
主要终点
To evaluate the oral bioavailability of investigational product (β-alanine complex (400 mg)), reference product I (Conventional β-alanine (400 mg)) and reference product II (Conventional β-alanine (1200 mg)) in healthy, adult, Human participants under fasting conditions

研究概览

简要总结

β-Alanine (or beta-alanine) [3-aminopropanoic acid] is a naturally occurring beta amino acid, which is an amino acid in which the amino group is attached to the β-carbon. BA, a precursor of carnosine, has been shown to increase intracellular levels of carnosine and reduce acidosis during high-intensity exercise. This indicates that carnosine may act as a physiologically meaningful physiochemical buffer. In normal conditions, rate of BA production is relatively low and serum BA concentration is undetectable. If there is an increase in BA to a detectable level in the bloodstream, there may also be a subsequent increase in carnosine in the muscle. This increase has been considered as enhancing blood buffering capacity and decreasing neuromuscular fatigue. Thus, the rationale of supplementing with BA as an ergogenic aid has often been described to increase athletic performance.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant and Investigator Blinded

入排标准

年龄范围
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • 1.Normal healthy adult male and female human subjects of age between 18-65 years with a body mass index (BMI) range between 18.50 kg/m2 to 24.99 kg/m2 2.Subject agrees avoid ß-alanine containing medications and dietary supplements from screening until last visit.
  • 3.Subject agrees to avoid high activity physical exercise 72.00 hours prior to last visit 4.Subjects who have no evidence of underlying disease during screening and check-in and whose screening is performed within 29 days of check in.

排除标准

  • 1.Evidence of allergy or known hypersensitivity to ß-alanine or other related drugs or other related drugs.
  • 2.Subjects with hepatic encephalopathy, cholestasis, myasthenia, pre-existing liver disease, alcohol abuse, existing tinnitus, renal or liver impairment and pre-existing gallbladder disease.
  • 3.Any major illness in the last three months or any significant ongoing chronic medical illness.
  • 4.Any disease or condition which might compromise the haemopoeitic, gastrointestinal, renal, hepatic, cardiovascular, Musculoskeletal, respiratory, central nervous system, diabetes, psychosis or any other body system.
  • 5.History of alcohol addiction or abuse.
  • 6.Malabsorption syndrome that affects β-alanine metabolism.

结局指标

主要结局

To evaluate the oral bioavailability of investigational product (β-alanine complex (400 mg)), reference product I (Conventional β-alanine (400 mg)) and reference product II (Conventional β-alanine (1200 mg)) in healthy, adult, Human participants under fasting conditions

时间窗: day 1

次要结局

  • To monitor the adverse events and to ensure the safety of the subjects.(da1, day30)

研究者

发起方
Natural Alternatives International
申办方类型
Pharmaceutical industry-Global
责任方
Principal Investigator
主要研究者

Dr Ambanna Gowda

Unitree Health Care Diagnostics

研究点 (1)

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