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Could a brief nerve squeeze improve lung surgery recovery?
NCT ID NCT07259031
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at whether briefly pressing on the phrenic nerve during lung surgery could help reduce complications like air leaks. Researchers compared 55 patients who had this temporary nerve compression with those who did not. They measured diaphragm activity, lung function, and recovery times to see if the technique is safe and effective.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this approach could offer a way to reduce complications like prolonged air leaks after lung surgery.
- What could go wrong
- This is a small, completed study with only 55 participants, so results may not apply to everyone. The nerve compression is temporary but could still cause unexpected side effects.
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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55 people
The number who actually took part.
- Started
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Sep 2019
- Finished
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Jun 2023
- 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 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.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adult patients (18+) who underwent lobectomy via muscle sparing thoracotomy * Patients with adequate preoperative pulmonary function to tolerate lobectomy * Patients who provided written informed consent for participation. * Patients with available postoperative follow-up data, including EMG and pulmonary function tests Exclusion Criteria: * Patients who underwent wedge resection, segmentectomy, pneumonectomy, or VATS procedures * Patients with previous phrenic nerve injury, diaphragmatic paralysis, or neuromuscular disorders affecting respiratory muscles. * Patients with incomplete postoperative follow-up or missing EMG/PFT data
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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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Konya City Hospital, Department of Thoracic Surgery
Konya, Konya, 42080, Turkey (Türkiye)
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