Heat therapy for lungs shows promise in severe asthma
NCT ID NCT02618551
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a procedure called bronchial thermoplasty for people with severe asthma that is not controlled by standard treatments. The treatment uses heat to thin the airway muscles, aiming to reduce breathlessness during exercise. 14 participants were enrolled, and the main goal was to see if the treatment improved lung function during physical activity.
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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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14 people
The number who actually took part.
- Start date
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Nov 2015
- Finished
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May 2021
- 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: * Severe asthma, uncontrolled despite optimal treatment according to GINA (global initiative for asthma) recommendations * At least 2 exacerbations treated by systemic steroids in the last year * FEV1 between 40 and 80% of predicted values and dynamic hyperinflation (defined as a decrease in inspiratory capacity by more than 500 ml during exercise) Exclusion Criteria: * Current asthma exacerbation or respiratory infection * History of exacerbation after bronchoscopy * FEV1 \< 40% of predicted values * Oxygen saturation \< 90% * Contra-indications to ALAIR catheter system : pacemaker or other electronic implanted device * Allergy to Remifentanyl or Propofol * pregnancy; breastfeeding
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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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DIDIER Alain
Toulouse, Midi Pyrenees, 31059, France
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