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Comparison of Exsufflation Versus Drainage in Primary Spontaneous Pneumothorax

Comparison of Efficacity of Simple Aspiration Versus Standard Drainage in the Management of Large Size Primary Spontaneous Pneumothorax

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01008228
Acronym
EXPRED
Enrollment
402
Registered
2009-11-05
Start date
2009-06-30
Completion date
2015-12-31
Last updated
2020-02-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pneumothorax

Keywords

spontaneous, primary, first episode

Brief summary

Management of primary spontaneous pneumothorax (PSP) remains unclear. Primary therapeutic goals for PSP include removal of air from the pleural space an prevention of recurrences. The absence of generally accepted and methodologically sound recommendations may account for the extensive variation in practice for air evacuation techniques. Air evacuation may be achieved by simple aspiration (exsufflation) or conventional chest tube drainage. Chest tube thoracotomy remains the most popular technique.Aspiration is a more simple technique, that allows possibility of ambulatory management. The purpose of the present study is to compare simple aspiration performed with a specific thoracentesis device, versus conventional chest tube drainage. Comparison will be performed on immediate efficacity of resolution of the pneumothorax.The hypothesis is that simple aspiration performed with a specific device is not inferior to chest tube drainage for management of a first episode of large size primary spontaneous pneumothorax. A second goal is to measure the efficacy at one week, and the recidive at one year. The trial is randomized, controlled and will include 200 patients for each group. The patients will be enrolled in 29 hospitals in France. Emergency department, thoracic surgery and pulmonary departments of each hospital were primarily contacted for agreement to participate to the study.

Interventions

PROCEDUREexsufflation

exsufflation will be performed with a specific thoracentesis system after introducing the device into chest pneumothorax, aspiration will be performed during 30 minutes

PROCEDUREthoracic tube drainage

thoracic tube drainage will be performed with a tube Ch 16 or ch 20

Sponsors

Centre Hospitalier Universitaire Dijon
CollaboratorOTHER
Belfort Hospital
CollaboratorOTHER
Central Hospital, Nancy, France
CollaboratorOTHER
Norman Bethune Medical Hospital
CollaboratorOTHER
St Philibert Hospital, Lomme
CollaboratorUNKNOWN
Hospital of Montfermeil
CollaboratorUNKNOWN
University Hospital, Brest
CollaboratorOTHER
University Hospital, Clermont-Ferrand
CollaboratorOTHER
Nantes University Hospital
CollaboratorOTHER
Association Hospitalière Nord Artois Cliniques
CollaboratorOTHER
Poitiers University Hospital
CollaboratorOTHER
University Hospital, Tours
CollaboratorOTHER
CHU de Reims
CollaboratorOTHER
Centre hospitalier de Perpignan
CollaboratorOTHER
Hospices Civils de Lyon
CollaboratorOTHER
Centre Hospitalier Universitaire de Saint Etienne
CollaboratorOTHER
Hospital of Roubaix
CollaboratorUNKNOWN
Hospital of Boulogne/mer
CollaboratorUNKNOWN
Assistance Publique Hopitaux De Marseille
CollaboratorOTHER
University Hospital, Rouen
CollaboratorOTHER
University Hospital, Angers
CollaboratorOTHER_GOV
Centre Hospitalier le Mans
CollaboratorOTHER
Centre Hospitalier Universitaire de Nīmes
CollaboratorOTHER
University Hospital, Grenoble
CollaboratorOTHER
Hospital of Mulhouse
CollaboratorUNKNOWN
Hospital of Valence
CollaboratorUNKNOWN
Centre Hospitalier Universitaire de Besancon
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* patients aged more than 18 years and less than 50 years * first episode of pneumothorax * primary pneumothorax (absence of known pulmonary disease) * large size of pneumothorax : presence of a visible rim of air between the lund margin and the chest wall, from the apex to pulmonary base

Exclusion criteria

* impossibility to obtain patient consent for psychiatric disease * patients under justice control * âgé less than 18 years, or more than 50 years * impossibility of medical follow de for geographic, social or psychic reasons * pregnant women * pneumothorax with acute respiratory insufficiency or bad tolerated * recidive of pneumothorax * traumatic pneumothorax * pneumothorax with pleural effusion * bilatéral pneumothorax * pneumothorax with pulmonary disease

Design outcomes

Primary

MeasureTime frame
size of residual pneumothorax measured on chest radiographyone day

Secondary

MeasureTime frame
size of residual pneumothorax at one weekone week
recidive of pneumothorax at one yearone year

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 10, 2026