Can a simple amino acid drink help elderly COPD patients keep muscle?
NCT ID NCT01173354
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether a special essential amino acid supplement (high in leucine) could help elderly patients with COPD build muscle protein better than a standard amino acid mixture. Thirty-four participants received a one-time dose of either supplement, and researchers measured changes in protein synthesis and breakdown. The goal was to see if targeting specific metabolic issues could improve muscle health in COPD.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- essential amino acid mixture (high leucine)
- What this could lead to
- If it works, this could point toward a nutritional supplement to help prevent muscle loss in elderly COPD patients.
- What could go wrong
- This is a very small, early study (34 people) looking only at short-term effects. It does not test long-term benefits or safety, so results may not lead to a practical treatment.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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34 people
The number who actually took part.
- Started
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Sep 2009
- Finished
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Feb 2012
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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45 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Diagnosis of chronic airflow limitation, defined as measured forced expiratory volume in one second (FEV1) less than 70% of reference FEV1 * Shortness of breath on exertion * Age 45 years and older * Clinically stable condition and not suffering from respiratory tract infection or exacerbation of their disease (defined as a combination of increased cough, sputum purulence, shortness of breath, systemic symptoms such as fever, and a decrease in FEV1 \> 10% compared with values when clinically stable in the preceding year) at least 4 weeks prior to the study * Ability to lie in supine position for 6 hours Exclusion Criteria: * Established diagnosis of malignancy * Presence of fever within the last 3 days * Established diagnosis of Diabetes Mellitus * Untreated metabolic diseases including hepatic or renal disorder * Presence of acute illness or metabolically unstable chronic illness * Recent myocardial infarction (less than 1 year) * Use of long-term oral corticosteroids or short course of oral corticosteroids in the preceding month before enrollment * Any other condition according to the PI or study physicians would interfere with proper conduct of the study / safety of the patient * Failure to give informed consent
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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University of Arkansas for Medical Sciences
Little Rock, Arkansas, 72205, United States
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