Acupuncture needles aim to boost lung recovery after surgery
NCT ID NCT07443540
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether adding acupuncture to standard breathing exercises helps people recover lung function after surgery to remove a lung nodule. Half of the 56 participants will get acupuncture plus usual care, while the other half gets usual care alone. Lung function, pain, and breathing will be measured one week after surgery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Acupuncture
- What this could lead to
- If it works, this could point toward a simple, drug-free way to help people breathe better and recover faster after lung surgery.
- What could go wrong
- This is a small, early-stage trial with only 56 people. Acupuncture may not provide significant benefit over standard breathing exercises alone.
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
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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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About 56 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Apr 2026
An estimate. Start dates often move.
- Expected to finish
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Jan 2027
An estimate. End dates often move.
- 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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18 to 65 years
- 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: \- Patients aged between 18 and 65 years. Diagnosed with a single pulmonary lesion (e.g., solitary pulmonary nodule or adenocarcinoma in situ). Scheduled to undergo elective wedge resection for the lung lesion. Exclusion Criteria: * History of prior lung resection. Medical history of asthma or pulmonary tuberculosis. History of pneumothorax prior to the current surgery. Expectation to receive rehabilitation therapies other than the standard protocol-defined incentive spirometry during the study period. Presence of other major systemic diseases (e.g., severe cardiovascular, renal, or hepatic impairment) that, in the investigator's opinion, render the patient unsuitable for trial 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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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