Neuromuscular Diseases (NMD)MYOPNEUMONCT07909018
Incidence and Risk Factors of Pneumothorax in Patients With Neuromuscular Diseases
An observational study of Neuromuscular Diseases (NMD) and Pneumothorax, run by Assistance Publique - Hôpitaux de Paris at 1 site in France.
Trial summary
Neuromuscular diseases can cause weakness of the respiratory muscles, leading to respiratory pump failure and respiratory insufficiency. Compensation for respiratory pump weakness and/or impaired cough is achieved using devices that apply pressure to increase airflow and ensure effective ventilation. Read more about this study
- Who is it for?
- Any age
- Conditions the study is for
- Neuromuscular Diseases (NMD), Pneumothorax
- What is being tested?
- Cough assistance device and/or thoracic mobilization and/or mechanical ventilation
- How many people
- 31,202 participants
- Where
- 1 siteFrance
- Study dates
- 29 Jan 2026to 29 Jan 2026
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Any age
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Study population: Patients (adults and children) with neuromuscular diseases hospitalised in one of the neuromuscular rare disease reference centers of Assistance Publique - Hôpitaux de Paris (Centre de Référence Maladies Rares neuromusculaires - CRMR Nord-Est- Île de France) (Chidren: Hôpital Raymond Poincaré, Hôpital Trousseau, Hôpital Necker ; Adults : Hôpital Raymond Poincaré, Hôpital Henri Mondor, Hôpital Pitié Salpêtrière) between July 1, 2017 and Décember 31, 2025.
Who may be able to join
- Patients (adults and children) with neuromuscular diseases hospitalised in one of the neuromuscular rare disease reference centers of Assistance Publique - Hôpitaux de Paris (Centre de Référence Maladies Rares neuromusculaires - CRMR Nord-Est- Île de France) (Chidren: Hôpital Raymond Poincaré, Hôpital Trousseau, Hôpital Necker ; Adults : Hôpital Raymond Poincaré, Hôpital Henri Mondor, Hôpital Pitié Salpêtrière) between July 1, 2017 and Décember 31, 2025.
Who cannot join
- NA
Trial locations and contacts
1 site in 1 country.
France1 site
Unité de Recherche Clinique Paris Saclay, Le Kremlin-Bicêtre 94270
Le Kremlin-Bicêtre, 94270
About this study
Neuromuscular diseases can cause weakness of the respiratory muscles, leading to respiratory pump failure and respiratory insufficiency. Compensation for respiratory pump weakness and/or impaired cough is achieved using devices that apply pressure to increase airflow and ensure effective ventilation. This technique can cause pneumothorax (separation of the lung from the chest wall), which can have potentially serious consequences.
The investigators aim to determine whether pneumothorax is a frequent complication in this population. The results of this study would help optimize treatment and ensure the most appropriate prescription of these therapies.
Read the detailed description
Neuromuscular diseases (NMDs) can cause respiratory muscle weakness, leading to mechanical failure of the respiratory pump. As the disease progresses, patients are exposed to multiple respiratory complications, ranging from sleep disturbances and daytime fatigue, related to sleep disruption caused by alveolar hypoventilation, to pneumonia and acute respiratory failure, which may be life-threatening.
The standard treatment for this respiratory failure is long-term mechanical ventilation, which is recommended for patients with neuromuscular diseases by the French National Authority for Health (Haute Autorité de Santé, HAS) and by the various National Diagnostic and Care Protocols. Depending on the severity of the disease and the progression of respiratory symptoms, mechanical ventilation may be used either at night or both during the night and the day. Since the second half of the 20th century, mechanical ventilation has been the standard treatment for restrictive respiratory failure of neuromuscular origin. This treatment, which provides respiratory pump support, has improved survival in these patients, sometimes by several decades, as observed in Duchenne muscular dystrophy. This treatment, used both for acute respiratory failure in intensive care settings and for chronic restrictive respiratory failure of non-parietal origin, is delivered through the application of positive inspiratory pressure, either invasively or non-invasively.
However, the management of these patients is not limited to mechanical ventilation. Other devices delivering positive pressure are also used. Respiratory muscle involvement also affects patients' ability to cough and clear airway secretions, thereby increasing the risk of respiratory tract infections and secretion retention. In this context, mechanical cough-assist devices are used to improve patients' airway clearance capacity. These devices are mechanical insufflation-exsufflation systems that apply positive pressure during inspiration to increase the insufflated volume, followed by negative pressure to generate an increased expiratory flow capable of facilitating secretion clearance. This treatment has become a particularly important component of the management of these patients, who are especially vulnerable to respiratory infections.
Finally, pediatric patients face an additional challenge, as respiratory pump failure may impair lung and thoracic growth, particularly when disease progression occurs during the first years of life. In the absence of specific intervention, this may lead to chest deformities (for example, a "pear-shaped" thorax in infants with spinal muscular atrophy due to underdevelopment of the pulmonary apices and/or scoliosis of varying severity. Orthopedic deformities combined with respiratory muscle weakness lead to restrictive respiratory failure before the end of growth, requiring specific respiratory management including non-invasive ventilation (NIV) with high pressure levels . Daily lung hyperinflation sessions performed using pressure insufflation devices are also proposed to promote thoracic and pulmonary growth.
The use of these different types of devices (mechanical ventilation, mechanical insufflation-exsufflation devices, etc.) is associated with well-known complications, particularly the risk of barotrauma related to increased intrathoracic pressure during inspiration, which may expose patients to the risk of pneumothorax. The occurrence of such complications may be promoted by patient-related intrinsic factors, including underlying conditions such as chronic obstructive pulmonary disease (COPD), interstitial lung disease, or acute respiratory distress syndrome (ARDS), but may also be related to ventilation settings. Data on the complications of mechanical ventilation affecting the pulmonary parenchyma have been available for several decades, both from animal and human studies. However, these studies have mainly focused on acute ventilation in the context of the management of acute respiratory distress syndrome.
In contrast, there are very few data on these complications in the context of chronic respiratory failure treated with mechanical ventilation, which is the standard treatment for respiratory failure of neuromuscular origin. No prospective study has investigated this population to determine the incidence of barotrauma-related complications. The only reports identified in the literature are isolated case reports describing the occurrence of pneumothorax in patients with Duchenne muscular dystrophy, amyotrophic lateral sclerosis, congenital nemaline myopathy , and Ullrich muscular dystrophy . These data do not allow investigators to determine whether there is an increased risk associated with positive-pressure respiratory support or whether specific diseases are at greater risk of developing pneumothorax. Furthermore, given the rarity of these diseases and their long-term course, conducting a prospective study involving a sufficiently large population of patients with neuromuscular diseases would be difficult.
The availability of access to data warehouses provides a new opportunity to address this question. The investigators aim to conduct a study using the AP-HP Health Data Warehouse (Entrepôt de Données de Santé, EDS) to analyze the prevalence of pneumothorax in a large population of patients with neuromuscular diseases and to assess its association with positive-pressure respiratory treatments, including mechanical ventilation, cough-assist devices (such as mechanical insufflation-exsufflation devices), and thoracic mobilization through lung hyperinflation (using pressure insufflation devices).
Working with data from the EDS would increase the statistical power of the sample. The vast majority of these patients receive multidisciplinary care in the neuromuscular rare disease reference centers within the FILNEMUS network. In the Île-de-France region, the six constituent centers of the neuromuscular rare disease reference center are located within the AP-HP (Pediatric centers: Trousseau, Necker, Raymond Poincaré; Adult centers: Pitié-Salpêtrière, Raymond Poincaré, Henri Mondor). The use of the AP-HP EDS will make it possible to analyze a large cohort capable of providing answers to these unresolved questions.
The investigators aim to determine the prevalence and frequency of pneumothorax in patients with neuromuscular diseases using these medical devices, and hypothesize that this prevalence is not higher than that observed in the general population.
The investigators also hypothesize that certain neuromuscular diseases, due to their pathophysiological characteristics, are associated with a higher risk of developing this type of adverse event.
Finally, exposure to mechanical ventilation and/or cough-assist devices and/or thoracic mobilization devices is hypothesized to be associated with an increased risk of pneumothorax. This study will provide objective data regarding the theoretical risk of a serious complication associated with respiratory devices that are widely prescribed in patients with neuromuscular diseases. If this study demonstrates that pneumothorax is a complication associated with neuromuscular diseases, it may encourage clinicians to monitor their patients more specifically by identifying those with disease-related risk factors. The results of this study will help guide the prescription of respiratory devices and allow the settings used to be adapted according to individual patient risk. Identifying neuromuscular diseases that are specifically associated with an increased risk of pneumothorax during respiratory support will make it possible to identify patients requiring specific adjustments and contribute to the appropriate prescription of these treatments. Identification of contributing risk factors may help limit the pressure levels prescribed in order to reduce the risk of complications.
The use of EDS data in the field of rare diseases represents an innovative approach to addressing unresolved clinical questions in these conditions, making it possible to collect a large amount of data over several years of follow-up. This represents a major asset for improving knowledge of these low-prevalence diseases, both in terms of determining their natural history and studying the consequences of their treatments.
- Conditions
- Neuromuscular Diseases (NMD), Pneumothorax
- Being tested
- Cough assistance device and/or thoracic mobilization and/or mechanical ventilation
- Keywords
- neuromuscular disease, pneumothorax
- Medical subject headings
- Neuromuscular Diseases, Pneumothorax
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Cough assistance device and/or thoracic mobilization and/or mechanical ventilationOther
Cough assistance device and/or thoracic mobilization and/or mechanical ventilation
| Study group | Role | What they receive |
|---|---|---|
| Patients with neuromuscular diseases hospitalised in reference centers of AP-HP | Patients (adults and children) with neuromuscular diseases hospitalised in one of the neuromuscular rare disease reference centers of Assistance Publique - Hôpitaux de Paris (Centre de Référence Maladies Rares neuromusculaires - CRMR Nord-Est- Île de France) (Chidren: Hôpital Raymond Poincaré, Hôpital Trousseau, Hôpital Necker ; Adults : Hôpital Raymond Poincaré, Hôpital Henri Mondor, Hôpital Pitié Salpêtrière) between July 1, 2017 and Décember 31, 2025. Receives: Other: Cough assistance device and/or thoracic mobilization and/or mechanical ventilation |
What is being measured
The primary outcome is the main question the study is designed to answer.
Incidence of pneumothorax diagnosis in patients with neuromuscular diseases overall and according to the type of neuromuscular disorder.
Number of new cases of pneumothorax per person-years in patients with neuromuscular disorders
Measured: From the date of admission to one of CRMR until the date of last follow-up or death in the reference center (up to 8 years)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted2 Nov 2026
- Study start29 Jan 2026
- Primary completion29 Jan 2026
- Study completion29 Jan 2026
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (16)Papers the sponsor has linked to this study.
- Other trials for Neuromuscular Diseases (NMD)Studies of the same condition, open and under way.
- More trials run by Assistance Publique - Hôpitaux de ParisThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Retrospective
- Enrolment
- 31,202 participants (actual)
Sponsor and investigators
- Lead sponsor
- Assistance Publique - Hôpitaux de Paris
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Hélène Prigent, Dr, Principal investigator, Explorations fonctionnelles - Hôpital Raymond Poincaré AP-HP
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07909018
- Sponsor's protocol ID
- CSE 25-0038
- Acronym
- MYOPNEUMO
- Status last verified
- Jan 2026
- First submitted
- 26 Oct 2026
- Last updated
- 4 Nov 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Fraser KL, Wong S, Foley AR, Chhibber S, Bonnemann CG, Lesser DJ, Grosmann C, Rutkowski A. Pneumothoraces in collagen VI-related dystrophy: a case series and recommendations for management. ERJ Open Res. 2017 Jun 23;3(2):00049-2017. doi: 10.1183/23120541.00049-2017. eCollection 2017 Apr.
PubMed 28660205Hino H, Suzuki Y, Ishii E, Fukuda M. Biphasic cuirass ventilation for treatment of an air leak after pneumothorax in a patient with nemaline myopathy: a case report. J Anesth. 2016 Dec;30(6):1087-1090. doi: 10.1007/s00540-016-2250-x. Epub 2016 Sep 19.
PubMed 27644222Park JS, Do YW, Park JM, Seok HY, Park D. Under-recognized primary spontaneous pneumothorax in ALS: a multicenter retrospective study. Neurol Sci. 2019 Dec;40(12):2509-2514. doi: 10.1007/s10072-019-03989-y. Epub 2019 Jul 2.
PubMed 31267304Cho HE, Byun J, Choi WA, Kim M, Kim KY, Kang SW. Analysis of Pneumothorax in Noninvasive Ventilator Users With Duchenne Muscular Dystrophy. Chest. 2021 Apr;159(4):1540-1547. doi: 10.1016/j.chest.2020.09.086. Epub 2020 Sep 19.
PubMed 32956714Vianello A, Arcaro G, Gallan F, Ori C, Bevilacqua M. Pneumothorax associated with long-term non-invasive positive pressure ventilation in Duchenne muscular dystrophy. Neuromuscul Disord. 2004 Jun;14(6):353-5. doi: 10.1016/j.nmd.2004.03.002.
PubMed 15145335Serpa Neto A, Cardoso SO, Manetta JA, Pereira VG, Esposito DC, Pasqualucci Mde O, Damasceno MC, Schultz MJ. Association between use of lung-protective ventilation with lower tidal volumes and clinical outcomes among patients without acute respiratory distress syndrome: a meta-analysis. JAMA. 2012 Oct 24;308(16):1651-9. doi: 10.1001/jama.2012.13730.
PubMed 23093163Amato MB, Barbas CS, Medeiros DM, Magaldi RB, Schettino GP, Lorenzi-Filho G, Kairalla RA, Deheinzelin D, Munoz C, Oliveira R, Takagaki TY, Carvalho CR. Effect of a protective-ventilation strategy on mortality in the acute respiratory distress syndrome. N Engl J Med. 1998 Feb 5;338(6):347-54. doi: 10.1056/NEJM199802053380602.
PubMed 9449727Boussarsar M, Thierry G, Jaber S, Roudot-Thoraval F, Lemaire F, Brochard L. Relationship between ventilatory settings and barotrauma in the acute respiratory distress syndrome. Intensive Care Med. 2002 Apr;28(4):406-13. doi: 10.1007/s00134-001-1178-1. Epub 2002 Jan 15.
PubMed 11967593Dreyfuss D, Soler P, Basset G, Saumon G. High inflation pressure pulmonary edema. Respective effects of high airway pressure, high tidal volume, and positive end-expiratory pressure. Am Rev Respir Dis. 1988 May;137(5):1159-64. doi: 10.1164/ajrccm/137.5.1159.
PubMed 3057957Thachuthara-George J. Pneumothorax in patients with respiratory failure in ICU. J Thorac Dis. 2021 Aug;13(8):5195-5204. doi: 10.21037/jtd-19-3752.
PubMed 34527359Chatwin M, Bush A, Simonds AK. Outcome of goal-directed non-invasive ventilation and mechanical insufflation/exsufflation in spinal muscular atrophy type I. Arch Dis Child. 2011 May;96(5):426-32. doi: 10.1136/adc.2009.177832. Epub 2010 Jun 23.
PubMed 20573738Ioos C, Leclair-Richard D, Mrad S, Barois A, Estournet-Mathiaud B. Respiratory capacity course in patients with infantile spinal muscular atrophy. Chest. 2004 Sep;126(3):831-7. doi: 10.1378/chest.126.3.831.
PubMed 15364763Kieny P, Chollet S, Delalande P, Le Fort M, Magot A, Pereon Y, Perrouin Verbe B. Evolution of life expectancy of patients with Duchenne muscular dystrophy at AFM Yolaine de Kepper centre between 1981 and 2011. Ann Phys Rehabil Med. 2013 Sep;56(6):443-54. doi: 10.1016/j.rehab.2013.06.002. Epub 2013 Jun 24.
PubMed 23876223Eagle M, Baudouin SV, Chandler C, Giddings DR, Bullock R, Bushby K. Survival in Duchenne muscular dystrophy: improvements in life expectancy since 1967 and the impact of home nocturnal ventilation. Neuromuscul Disord. 2002 Dec;12(10):926-9. doi: 10.1016/s0960-8966(02)00140-2.
PubMed 12467747Haute Autorité de Santé; Haute Autorité de Santé. Protocole National de Diagnostic et de Soins (PNDS) Myopathies reliées au collagène VI. 2022.
Study at a glance
From the registry record, last updated by the sponsor on 4 Nov 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Incidence and Risk Factors of Pneumothorax in Patients With Neuromuscular Diseases
- ClinicalTrials.gov ID
- NCT07909018
- Acronym / sponsor ID
- MYOPNEUMO / CSE 25-0038
- Conditions
- Neuromuscular Diseases (NMD), Pneumothorax
- Keywords
- neuromuscular disease, pneumothorax
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 31,202 participants (actual)
- Lead sponsor
- Assistance Publique - Hôpitaux de ParisUniversity, hospital or other
- Study start
- 29 Jan 2026 (actual)
- Primary completion
- 29 Jan 2026 (actual)
- Study completion
- 29 Jan 2026 (actual)
- First posted
- 2 Nov 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Neuromuscular diseases can cause weakness of the respiratory muscles, leading to respiratory pump failure and respiratory insufficiency. Compensation for respiratory pump weakness and/or impaired cough is achieved using devices that apply pressure to increase airflow and ensure effective ventilation. This technique can cause pneumothorax (separation of the lung from the chest wall), which can have potentially serious consequences.
The investigators aim to determine whether pneumothorax is a frequent complication in this population. The results of this study would help optimize treatment and ensure the most appropriate prescription of these therapies.
Detailed description
Neuromuscular diseases (NMDs) can cause respiratory muscle weakness, leading to mechanical failure of the respiratory pump. As the disease progresses, patients are exposed to multiple respiratory complications, ranging from sleep disturbances and daytime fatigue, related to sleep disruption caused by alveolar hypoventilation, to pneumonia and acute respiratory failure, which may be life-threatening.
The standard treatment for this respiratory failure is long-term mechanical ventilation, which is recommended for patients with neuromuscular diseases by the French National Authority for Health (Haute Autorité de Santé, HAS) and by the various National Diagnostic and Care Protocols. Depending on the severity of the disease and the progression of respiratory symptoms, mechanical ventilation may be used either at night or both during the night and the day. Since the second half of the 20th century, mechanical ventilation has been the standard treatment for restrictive respiratory failure of neuromuscular origin. This treatment, which provides respiratory pump support, has improved survival in these patients, sometimes by several decades, as observed in Duchenne muscular dystrophy. This treatment, used both for acute respiratory failure in intensive care settings and for chronic restrictive respiratory failure of non-parietal origin, is delivered through the application of positive inspiratory pressure, either invasively or non-invasively.
However, the management of these patients is not limited to mechanical ventilation. Other devices delivering positive pressure are also used. Respiratory muscle involvement also affects patients' ability to cough and clear airway secretions, thereby increasing the risk of respiratory tract infections and secretion retention. In this context, mechanical cough-assist devices are used to improve patients' airway clearance capacity. These devices are mechanical insufflation-exsufflation systems that apply positive pressure during inspiration to increase the insufflated volume, followed by negative pressure to generate an increased expiratory flow capable of facilitating secretion clearance. This treatment has become a particularly important component of the management of these patients, who are especially vulnerable to respiratory infections.
Finally, pediatric patients face an additional challenge, as respiratory pump failure may impair lung and thoracic growth, particularly when disease progression occurs during the first years of life. In the absence of specific intervention, this may lead to chest deformities (for example, a "pear-shaped" thorax in infants with spinal muscular atrophy due to underdevelopment of the pulmonary apices and/or scoliosis of varying severity. Orthopedic deformities combined with respiratory muscle weakness lead to restrictive respiratory failure before the end of growth, requiring specific respiratory management including non-invasive ventilation (NIV) with high pressure levels . Daily lung hyperinflation sessions performed using pressure insufflation devices are also proposed to promote thoracic and pulmonary growth.
The use of these different types of devices (mechanical ventilation, mechanical insufflation-exsufflation devices, etc.) is associated with well-known complications, particularly the risk of barotrauma related to increased intrathoracic pressure during inspiration, which may expose patients to the risk of pneumothorax. The occurrence of such complications may be promoted by patient-related intrinsic factors, including underlying conditions such as chronic obstructive pulmonary disease (COPD), interstitial lung disease, or acute respiratory distress syndrome (ARDS), but may also be related to ventilation settings. Data on the complications of mechanical ventilation affecting the pulmonary parenchyma have been available for several decades, both from animal and human studies. However, these studies have mainly focused on acute ventilation in the context of the management of acute respiratory distress syndrome.
In contrast, there are very few data on these complications in the context of chronic respiratory failure treated with mechanical ventilation, which is the standard treatment for respiratory failure of neuromuscular origin. No prospective study has investigated this population to determine the incidence of barotrauma-related complications. The only reports identified in the literature are isolated case reports describing the occurrence of pneumothorax in patients with Duchenne muscular dystrophy, amyotrophic lateral sclerosis, congenital nemaline myopathy , and Ullrich muscular dystrophy . These data do not allow investigators to determine whether there is an increased risk associated with positive-pressure respiratory support or whether specific diseases are at greater risk of developing pneumothorax. Furthermore, given the rarity of these diseases and their long-term course, conducting a prospective study involving a sufficiently large population of patients with neuromuscular diseases would be difficult.
The availability of access to data warehouses provides a new opportunity to address this question. The investigators aim to conduct a study using the AP-HP Health Data Warehouse (Entrepôt de Données de Santé, EDS) to analyze the prevalence of pneumothorax in a large population of patients with neuromuscular diseases and to assess its association with positive-pressure respiratory treatments, including mechanical ventilation, cough-assist devices (such as mechanical insufflation-exsufflation devices), and thoracic mobilization through lung hyperinflation (using pressure insufflation devices).
Working with data from the EDS would increase the statistical power of the sample. The vast majority of these patients receive multidisciplinary care in the neuromuscular rare disease reference centers within the FILNEMUS network. In the Île-de-France region, the six constituent centers of the neuromuscular rare disease reference center are located within the AP-HP (Pediatric centers: Trousseau, Necker, Raymond Poincaré; Adult centers: Pitié-Salpêtrière, Raymond Poincaré, Henri Mondor). The use of the AP-HP EDS will make it possible to analyze a large cohort capable of providing answers to these unresolved questions.
The investigators aim to determine the prevalence and frequency of pneumothorax in patients with neuromuscular diseases using these medical devices, and hypothesize that this prevalence is not higher than that observed in the general population.
The investigators also hypothesize that certain neuromuscular diseases, due to their pathophysiological characteristics, are associated with a higher risk of developing this type of adverse event.
Finally, exposure to mechanical ventilation and/or cough-assist devices and/or thoracic mobilization devices is hypothesized to be associated with an increased risk of pneumothorax. This study will provide objective data regarding the theoretical risk of a serious complication associated with respiratory devices that are widely prescribed in patients with neuromuscular diseases. If this study demonstrates that pneumothorax is a complication associated with neuromuscular diseases, it may encourage clinicians to monitor their patients more specifically by identifying those with disease-related risk factors. The results of this study will help guide the prescription of respiratory devices and allow the settings used to be adapted according to individual patient risk. Identifying neuromuscular diseases that are specifically associated with an increased risk of pneumothorax during respiratory support will make it possible to identify patients requiring specific adjustments and contribute to the appropriate prescription of these treatments. Identification of contributing risk factors may help limit the pressure levels prescribed in order to reduce the risk of complications.
The use of EDS data in the field of rare diseases represents an innovative approach to addressing unresolved clinical questions in these conditions, making it possible to collect a large amount of data over several years of follow-up. This represents a major asset for improving knowledge of these low-prevalence diseases, both in terms of determining their natural history and studying the consequences of their treatments.
Study design
- Observational model
- Cohort
- Time perspective
- Retrospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Patients with neuromuscular diseases hospitalised in reference centers of AP-HP | – | Other: Cough assistance device and/or thoracic mobilization and/or mechanical ventilationPatients (adults and children) with neuromuscular diseases hospitalised in one of the neuromuscular rare disease reference centers of Assistance Publique - Hôpitaux de Paris (Centre de Référence Maladies Rares neuromusculaires - CRMR Nord-Est- Île de France) (Chidren: Hôpital Raymond Poincaré, Hôpital Trousseau, Hôpital Necker ; Adults : Hôpital Raymond Poincaré, Hôpital Henri Mondor, Hôpital Pitié Salpêtrière) between July 1, 2017 and Décember 31, 2025. |
Who may qualify
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
- Study population
- Patients (adults and children) with neuromuscular diseases hospitalised in one of the neuromuscular rare disease reference centers of Assistance Publique - Hôpitaux de Paris (Centre de Référence Maladies Rares neuromusculaires - CRMR Nord-Est- Île de France) (Chidren: Hôpital Raymond Poincaré, Hôpital Trousseau, Hôpital Necker ; Adults : Hôpital Raymond Poincaré, Hôpital Henri Mondor, Hôpital Pitié Salpêtrière) between July 1, 2017 and Décember 31, 2025.
Key inclusion criteria (1 listed)
- Patients (adults and children) with neuromuscular diseases hospitalised in one of the neuromuscular rare disease reference centers of Assistance Publique - Hôpitaux de Paris (Centre de Référence Maladies Rares neuromusculaires - CRMR Nord-Est- Île de France) (Chidren: Hôpital Raymond Poincaré, Hôpital Trousseau, Hôpital Necker ; Adults : Hôpital Raymond Poincaré, Hôpital Henri Mondor, Hôpital Pitié Salpêtrière) between July 1, 2017 and Décember 31, 2025.
Key exclusion criteria (1 listed)
- NA
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Cough assistance device and/or thoracic mobilization and/or mechanical ventilationCough assistance device and/or thoracic mobilization and/or mechanical ventilation | Other | Patients with neuromuscular diseases hospitalised in reference centers of AP-HP |
Primary outcome
Incidence of pneumothorax diagnosis in patients with neuromuscular diseases overall and according to the type of neuromuscular disorder.
Time frame: From the date of admission to one of CRMR until the date of last follow-up or death in the reference center (up to 8 years)
Number of new cases of pneumothorax per person-years in patients with neuromuscular disorders
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 4 Nov 2026.
- Background: PubMed 28660205Fraser KL, Wong S, Foley AR, Chhibber S, Bonnemann CG, Lesser DJ, Grosmann C, Rutkowski A. Pneumothoraces in collagen VI-related dystrophy: a case series and recommendations for management. ERJ Open Res. 2017 Jun 23;3(2):00049-2017. doi: 10.1183/23120541.00049-2017. eCollection 2017 Apr.
- Background: PubMed 27644222Hino H, Suzuki Y, Ishii E, Fukuda M. Biphasic cuirass ventilation for treatment of an air leak after pneumothorax in a patient with nemaline myopathy: a case report. J Anesth. 2016 Dec;30(6):1087-1090. doi: 10.1007/s00540-016-2250-x. Epub 2016 Sep 19.
- Background: PubMed 31267304Park JS, Do YW, Park JM, Seok HY, Park D. Under-recognized primary spontaneous pneumothorax in ALS: a multicenter retrospective study. Neurol Sci. 2019 Dec;40(12):2509-2514. doi: 10.1007/s10072-019-03989-y. Epub 2019 Jul 2.
- Background: PubMed 32956714Cho HE, Byun J, Choi WA, Kim M, Kim KY, Kang SW. Analysis of Pneumothorax in Noninvasive Ventilator Users With Duchenne Muscular Dystrophy. Chest. 2021 Apr;159(4):1540-1547. doi: 10.1016/j.chest.2020.09.086. Epub 2020 Sep 19.
- Background: PubMed 15145335Vianello A, Arcaro G, Gallan F, Ori C, Bevilacqua M. Pneumothorax associated with long-term non-invasive positive pressure ventilation in Duchenne muscular dystrophy. Neuromuscul Disord. 2004 Jun;14(6):353-5. doi: 10.1016/j.nmd.2004.03.002.
- Background: PubMed 23093163Serpa Neto A, Cardoso SO, Manetta JA, Pereira VG, Esposito DC, Pasqualucci Mde O, Damasceno MC, Schultz MJ. Association between use of lung-protective ventilation with lower tidal volumes and clinical outcomes among patients without acute respiratory distress syndrome: a meta-analysis. JAMA. 2012 Oct 24;308(16):1651-9. doi: 10.1001/jama.2012.13730.
- Background: PubMed 9449727Amato MB, Barbas CS, Medeiros DM, Magaldi RB, Schettino GP, Lorenzi-Filho G, Kairalla RA, Deheinzelin D, Munoz C, Oliveira R, Takagaki TY, Carvalho CR. Effect of a protective-ventilation strategy on mortality in the acute respiratory distress syndrome. N Engl J Med. 1998 Feb 5;338(6):347-54. doi: 10.1056/NEJM199802053380602.
- Background: PubMed 11967593Boussarsar M, Thierry G, Jaber S, Roudot-Thoraval F, Lemaire F, Brochard L. Relationship between ventilatory settings and barotrauma in the acute respiratory distress syndrome. Intensive Care Med. 2002 Apr;28(4):406-13. doi: 10.1007/s00134-001-1178-1. Epub 2002 Jan 15.
- Background: PubMed 3057957Dreyfuss D, Soler P, Basset G, Saumon G. High inflation pressure pulmonary edema. Respective effects of high airway pressure, high tidal volume, and positive end-expiratory pressure. Am Rev Respir Dis. 1988 May;137(5):1159-64. doi: 10.1164/ajrccm/137.5.1159.
- Background: PubMed 34527359Thachuthara-George J. Pneumothorax in patients with respiratory failure in ICU. J Thorac Dis. 2021 Aug;13(8):5195-5204. doi: 10.21037/jtd-19-3752.
- Background: PubMed 20573738Chatwin M, Bush A, Simonds AK. Outcome of goal-directed non-invasive ventilation and mechanical insufflation/exsufflation in spinal muscular atrophy type I. Arch Dis Child. 2011 May;96(5):426-32. doi: 10.1136/adc.2009.177832. Epub 2010 Jun 23.
- Background: PubMed 15364763Ioos C, Leclair-Richard D, Mrad S, Barois A, Estournet-Mathiaud B. Respiratory capacity course in patients with infantile spinal muscular atrophy. Chest. 2004 Sep;126(3):831-7. doi: 10.1378/chest.126.3.831.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Hélène Prigent, Dr principal investigator
Explorations fonctionnelles - Hôpital Raymond Poincaré AP-HP
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Neuromuscular Diseases (NMD) and Pneumothorax, run by Assistance Publique - Hôpitaux de Paris at 1 site in France.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 4 Nov 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Incidence of pneumothorax diagnosis in patients with neuromuscular diseases overall and according to the type of neuromuscular disorder. (time frame: From the date of admission to one of CRMR until the date of last follow-up or death in the reference center (up to 8 years)). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT07909018, which also lists 16 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 Nov 2026.