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Acetaminophen and Impaired Musculoskeletal Adaptations to Exercise Training

University of Colorado Denver (CU Denver) logo

University of Colorado Denver (CU Denver)

Status

Completed

Conditions

Osteoporosis
Aging
Sarcopenia

Treatments

Behavioral: Resistance training

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT01083901
06-0343
R21AG027809 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

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.

Full description

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.

Enrollment

34 patients

Sex

Male

Ages

50+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 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

Exclusion criteria

  • 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

Trial design

34 participants in 3 patient groups, including a placebo group

Resistance training with Acetaminophen
Experimental group
Description:
Acetaminophen
Treatment:
Behavioral: Resistance training
Resistance Training with ibuprofen
Experimental group
Description:
Ibuprofen
Treatment:
Behavioral: Resistance training
placebo
Placebo Comparator group
Description:
Placebo
Treatment:
Behavioral: Resistance training

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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