Study Designed to Optimize the Treatment of Primary Pneumothorax (TOPP)
Primary Spontaneous Pneumothorax, Pleural Disease
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About this trial
This is an interventional treatment trial for Primary Spontaneous Pneumothorax focused on measuring primary spontaneous pneumothorax, epidemiology, genetics, risk factors
Eligibility Criteria
Inclusion Criteria:
- First incidence of primary spontaneous pneumothorax.
- Age between 18 and 40.
- No known preexisting pulmonary disease.
- Patient must accept randomization.
- Able to read and understand information regarding the study.
- The condition must require treatment with a chest-tube.
Exclusion Criteria:
- Age above 40.
- Previously pulmonary og cardiac surgery.
- Pregnant or breastfeeding.
- Patients who do not tolerate anesthetics.
Sites / Locations
- Research Unit at the cardiothoracic departement at the University Hospital of OdenseRecruiting
- Research Unit at the Cardiothoracic Department at the University Hospital of SkejbyRecruiting
- Research Unit at the Cardiothoracic Department af Ålborg HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Experimental
Experimental
Experimental
Experimental
HRCT with bullae, treatment conservative
HRCT no bullae, treatment conservative
HRCT with bullae, treatment VATS.
HRCT no bullae, treatment VATS.
Patients undergo High-resolution CT scan, and significant bullae are identified (i.e. > 1 cm). Afterwards randomised to conservative treatment with conventional chest-tube drainage.
Patients undergo High-resolution CT scan, and no significant bullae are identified (i.e. > 1 cm). Afterwards randomised to conservative treatment with conventional chest-tube drainage.
Patients undergo High-resolution CT scan, and significant bullae are identified (i.e. > 1 cm). Afterwards randomised to active treatment with VATS bullectomy and mechanical pleurodesis.
Patients undergo High-resolution CT scan, and no significant bullae are identified (i.e. > 1 cm). Afterwards randomised to active treatment with VATS bullectomy and mechanical pleurodesis.