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临床试验/NCT02770417
NCT02770417已完成不适用

Oral β-Alanine Supplementation in Patients With COPD: Structural, Metabolic and Functional Adaptations

Hasselt University2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2016年5月1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
60
试验地点
2
主要终点
muscle carnosine

研究概览

简要总结

Preliminary evidence suggest that patients with chronic obstructive pulmonary disease (COPD) suffer from lower-limb muscle dysfunction. This may, at least in part, be due to a combination of physical inactivity and muscle oxidative stress. Pilot data (not published) clearly show that patients with COPD have significantly lower carnosine, which is a pH (acidity-basicity level) buffer and antioxidant, levels in the m. vastus lateralis compared to healthy subjects. Beta-alanine supplementation has shown to increase muscle carnosine in trained and untrained healthy subjects. This study will assess if muscle carnosine can be augmented by beta-alanine supplementation in 40 COPD patients (20 patients receive beta-alanine, 20 patients receive placebo). 10 healthy elderly controls will also be assessed to compare baseline muscle carnosine levels.

The aims of this study are to:

  1. Investigate baseline muscle carnosine levels to confirm the pilot data in a larger sample of patients with COPD compared with healthy elderly subjects
  2. Investigate if beta-alanine supplementation augments muscle carnosine in COPD patients and whether it has an influence on exercise capacity, lower-limb muscle function and quality of life
  3. To investigate baseline and post supplementation structural and metabolic muscle characteristics and markers of oxidative stress and inflammation in COPD patients and it's association with muscle carnosine levels

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)

入排标准

年龄范围
40 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • COPD: diagnosis of moderate to very severe COPD according to Global Initiative for Chronic Obstructive Lung Disease (GOLD) guidelines
  • Healthy controls: forced expiratory volume at one second/forced vital capacity (FEV1/FVC) > 0.7, matched for age and gender

排除标准

  • The presence of known instable cardiac disease
  • neurological disease and/or musculoskeletal disease that preclude safe participation in an exercise test
  • a history of drugs/alcohol abuse
  • vegetarianism
  • inability to understand the Flemish language.
  • COPD-specific exclusion criteria:
  • COPD exacerbation and/or hospitalization in the last 6 weeks
  • participation in pulmonary rehabilitation in the previous 12 months.

研究组 & 干预措施

Healthy controls

Other

干预措施: control (Other)

COPD (placebo)

Placebo Comparator

干预措施: placebo (Dietary Supplement)

COPD (beta-alanine)

Active Comparator

干预措施: beta-alanine (Dietary Supplement)

结局指标

主要结局

muscle carnosine

时间窗: change from baseline to 12 weeks

by means of high pressure liquid chromatography(HPLC)-analysis of a muscle biopsy

maximal exercise capacity

时间窗: change from baseline to 12 weeks

by means of an incremental maximal cycle test

submaximal exercise capacity

时间窗: change from baseline to 12 weeks

by means of a constant-work rate cycle test

次要结局

  • Functional exercise test 2(change from baseline to 12 weeks)
  • Muscle function hand grip(change from baseline to 12 weeks)
  • Functional exercise test 1(change from baseline to 12 weeks)
  • Muscle function quadriceps(change from baseline to 12 weeks)
  • Blood parameters maximal exercise test(change from baseline to 12 weeks)
  • Quality of life: general(change from baseline to 12 weeks)
  • Respiratory muscle function(change from baseline to 12 weeks)
  • Comorbidities: ankle-brachial pressure index(change from baseline to 12 weeks)
  • Comorbidities body composition 1(change from baseline to 12 weeks)
  • Comorbidities(change from baseline to 12 weeks)
  • Physical activity: questionnaire 1(change from baseline to 12 weeks)
  • Lung function(change from baseline to 12 weeks)
  • Muscle characteristics(change from baseline to 12 weeks)
  • Comorbidities blood pressure(change from baseline to 12 weeks)
  • Quality of life: fatigue(change from baseline to 12 weeks)
  • Blood parameters submaximal exercise test(change from baseline to 12 weeks)
  • Blood parameters fasted state(change from baseline to 12 weeks)
  • Quality of life: dyspnea(change from baseline to 12 weeks)
  • Heart function(change from baseline to 12 weeks)
  • Comorbidities body composition 2(change from baseline to 12 weeks)
  • Quality of life: anxiety and depression(change from baseline to 12 weeks)
  • Physical activity: accelerometer(change from baseline to 12 weeks)
  • Physical activity: questionnaire 2(change from baseline to 12 weeks)
  • Quality of life: COPD(change from baseline to 12 weeks)

研究者

发起方
Hasselt University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Martijn Spruit

prof. dr.

Hasselt University

研究点 (2)

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