Freezing nerves to fight pain after lung surgery: a new hope?
NCT ID NCT05348447
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests a technique called intercostal nerve cryotherapy, where doctors freeze nerves between the ribs during minimally invasive lung surgery to control pain afterward. About 110 adults having lung nodule removal will be randomly assigned to receive either the freezing treatment or standard pain control. The main goals are to see if cryotherapy reduces the amount of morphine needed and lowers pain scores.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Intercostal nerve cryotherapy (freezing nerves between ribs using a device)
- What this could lead to
- If it works, this could offer a new way to manage post-surgical pain with less need for strong painkillers like morphine.
- What could go wrong
- This is a small, early-stage trial (110 people) testing a procedure, not a drug. The freezing may not reduce pain enough to change standard care, and there could be side effects like nerve damage or prolonged numbness.
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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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110 people
The number who actually took part.
- Started
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Apr 2022
- Expected to finish
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Mar 2026
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 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: 1. Patients 18 year and older. 2. Undergoing elective minimally invasive (VATS or robotic) lung resection for nodules (wedge resection, segmentectomy, lobectomy). 3. Performance status of 1 or 2. Exclusion Criteria: 1. Patients with ejection fraction less than 40% 2. Patients with creatinine greater than 1.5. 3. Patients with Child's B or C cirrhosis 4. Patients on chronic narcotics for other reasons 5. Patients diagnosed with fibromyalgia 6. Patients who had previous thoracic surgery on the same side. 7. Patients who cannot communicate in English. 8. Patients unable to provide informed consent for the study.
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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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AHN Allegheny General Hospital
Pittsburgh, Pennsylvania, 15212, United States
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