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临床试验/NCT01083901
NCT01083901已完成不适用

Acetaminophen and Impaired Musculoskeletal Adaptations to Exercise Training

University of Colorado, Denver1 个研究点 分布在 1 个国家目标入组 34 人开始时间: 2006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
入组人数
34
试验地点
1
主要终点
Change in Total Body Fat-free Mass

研究概览

简要总结

The purpose of this study is to determine if taking the pain reliever acetaminophen (ACET) interferes with some of the benefits of weight lifting on muscles and bone density in older men.

详细描述

The commonly used pain relievers acetaminophen and ibuprofen may impair musculoskeletal adaptations to progressive resistance exercise training by inhibiting exercise-induced muscle protein synthesis.

To test the hypothesis that acetaminophen and ibuprofen would diminish training-induced increases in fat-free mass, untrained men (n=26) aged ≥ 50 years participated in 16 weeks of high-intensity progressive resistance exercise training and bone-loading exercises and were randomly assigned to take ACET (1000 mg), ibuprofen (400 mg) or placebo 2 hours before each exercise session.

The primary outcome was the change in total body fat-free mass measured by dual-energy X-ray absorptiometry (DXA) at baseline and week 16. Our primary interest was in the comparison of the acetaminophen and placebo groups.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
50 Years 至 —(Adult, Older Adult)
性别
Male
接受健康志愿者
是

入选标准

  • •average use of acetaminophen and non-steroidal anti-inflammatory drugs (NSAIDs) [including aspirin] less than 3 days per month
  • •not currently engaged in moderate-to-vigorous weight-lifting exercise
  • •non-smoker
  • •willing to participate in a supervised exercise program for 9 months

排除标准

  • •relative or absolute contraindications to regular use of acetaminophen or NSAIDs including known allergy or intolerance to either drug,history of peptic ulcer or GI bleeding, anemia, asthma with bronchospasm induced by aspirin or other NSAIDS, moderate or severe renal impairment, known hepatobiliary disease
  • •contraindications to exercise testing and training including congestive heart failure class III or IV, uncontrolled hypertension and unstable cardiovascular disease
  • •thyroid dysfunction
  • •orthopedic problems that limit the ability to perform vigorous exercise or increase the likelihood of the use of pain medications
  • •drugs known to alter bone metabolism
  • •allergy to lidocaine
  • •diabetes mellitus requiring pharmacologic therapy

研究组 & 干预措施

Resistance training with Acetaminophen

Experimental

Acetaminophen

干预措施: Resistance training (Behavioral)

Resistance Training with ibuprofen

Experimental

Ibuprofen

干预措施: Resistance training (Behavioral)

placebo

Placebo Comparator

Placebo

干预措施: Resistance training (Behavioral)

结局指标

主要结局

Change in Total Body Fat-free Mass

时间窗: 16 weeks

change from baseline to 16 weeks in fat-free mass measured by DXA (Hologic Discovery W, version 12.6)

次要结局

  • Change in Total Body Fat Mass(16 weeks)
  • Changes in Upper Body Strength.(16 weeks)
  • Change in Lower Body Strength(16 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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