Simple supplements may fight fatigue in advanced lung disease
NCT ID NCT06439875
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This study tested whether taking L-arginine and liposomal vitamin C supplements twice daily could reduce fatigue in people with COPD and chronic respiratory failure. 101 patients were randomly assigned to receive the supplements or a placebo during a 28-day pulmonary rehabilitation program. The main goal was to measure changes in fatigue severity using a standard questionnaire.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- L-arginine and liposomal vitamin C
- What this could lead to
- If it works, this could offer a simple supplement to ease fatigue and improve daily life for people with advanced COPD.
- What could go wrong
- This is a small, completed trial with no phase designation, so results may not be conclusive or widely applicable. Supplements may not work for everyone.
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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101 people
The number who actually took part.
- Started
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Jul 2024
- Finished
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Mar 2026
- 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
-
40 to 90 years
- Sex
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Anyone
- Healthy volunteers
-
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: * COPD patients of both sexes complicated by respiratory failure (PaO2 inferior to 60 mmHg while breathing room air) * aged between 40 and 90 years selected from the inpatient/outpatient population admitted to perform a PR program in 12 Italian rehabilitation hospitals. Exclusion criteria: * consuming any ergogenic supplement in the last 2 months; * severe acute exacerbations in the 3 months before enrolment; * clinical instability (pH inferior to 7.35, hemodynamic instability, tachypnea at rest); * lung restrictive diseases; * primitive pulmonary hypertension; * recent lung thromboembolic events; * orthopaedic clinical conditions interfering with exercise; * coronary heart disease; * cardiac failure with reduced ejection fraction; * major cardiac arrhythmias; * neuromuscular diseases; * mini mental state examination (MMSE) \<24; * any prior or current medical problem that would limit the subject participation
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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
-
Istituti Clinici Scientifici Maugeri IRCCS
Lumezzane, Brescia, 25065, Italy
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Istituti Clinici Scientifici Maugeri IRCCS
Bari, 70124, Italy
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Istituti Clinici Scientifici Maugeri Irccs
Telese Terme, Benevento, 82037, Italy
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