Funnel chest surgery: does it really improve breathing and heart health?
NCT ID NCT03770390
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at 43 people with funnel chest (pectus excavatum) to see how corrective surgery changes their heart and lung function during exercise and their overall quality of life. Researchers measured oxygen use, breathing, and symptoms like shortness of breath or heart fluttering before and after surgery. The goal was to understand the real benefits of the operation beyond just appearance.
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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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43 people
The number who actually took part.
- Started
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Dec 2018
- Finished
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Dec 2024
- 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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14 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: * Patient with pectus excavatum * The patient received corrective surgery within four years of enrollment and is scheduled for a follow-up visit --OR-- the patient is scheduled for corrective surgery during the inclusion period * Collection of informed written consent (patient and legal guardian, if applicable) * Obligation of affiliation or beneficiary of a social security programme Exclusion Criteria: * Impossibility for the patient to participate in his/her next annual follow-up visit * Absence of exercise test data AND respiratory function test data performed during the preoperative check-up * Subject in exclusion period required by another protocol * Pregnant or lactating woman, patient unable to give consent, protected adult, vulnerable persons (according to French Health Code articles L.1121-6, L.1121-7, L.1211-8, L.1211-9) * Subject deprived of liberty by judicial or administrative decision * Participation of the subject in another interventional protocol * Failure to properly inform the patient (e.g. a language barrier)
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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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Hôpital Arnaud de Villeneuve - CHU de Montpellier
Montpellier, 34295, France
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Other studies related to the condition(s) this trial covers.