Pneumothorax Clinical Trial
Official title:
Comparison of Chest Tube Drainage Versus Thoracoscopic Surgery for Unsuccessful Aspiration of Primary Spontaneous Pneumothorax: a Prospective Randomized Trial
We hypothesize that VATS is more effective than CTD for management of primary spontaneous pneumothorax with aspiration failure. To this end, we will compare two groups of patients who had experienced unsuccessful aspiration of primary spontaneous pneumothorax stratified by treatment.
Status | Recruiting |
Enrollment | 60 |
Est. completion date | September 2013 |
Est. primary completion date | November 2012 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 15 Years to 50 Years |
Eligibility |
Inclusion Criteria: 1. Age between 15 and 50 years old. 2. First episode of spontaneous pneumothorax. 3. The rim of air is > 2cm on CXR requiring simple aspiration 4. Aspiration as the initial treatment 5. Failed to achieve lung expansion following repeat manual aspiration Exclusion Criteria: 1. Complete or nearly complete and persistent lung expansion immediately following manual aspiration 2. With underlying pulmonary disease (TB, asthma, etc) 3. With hemothorax or tension pneumothorax requiring chest tube insertion or operation 4. A history of previous pneumothorax 5. A history of previous ipsilateral thoracic operation 6. Pregnant or lactation female |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Taiwan | National Taiwan University Hospital | Taipei | |
Taiwan | Far Eastern Memorial Hospital | Taipei county |
Lead Sponsor | Collaborator |
---|---|
National Taiwan University Hospital | Department of Health, Executive Yuan, R.O.C. (Taiwan) |
Taiwan,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Comparing the number of days in hospital, after intervention, of each group. | within one month | No | |
Secondary | Short-term outcome, including number of days with chest drainage, total hospital stay, short-term failure rate of assigned treatment, adverse events, pain score, mean dose of meperidine requested. | within one month | Yes | |
Secondary | Long-term outcome, including recurrence rate and long-term failure rate of assigned treatment | 2 years | No | |
Secondary | Total costs of each patients in assigned treatment. | 2 years | No |
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