*A prospective, randomised trial in pneumothorax therapy: manual aspiration versus conventional chest tube drainage.*
- Conditions
- lung rupturepneumothorax10035597
- Registration Number
- NL-OMON30187
- Lead Sponsor
- Isala Klinieken
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 114
1.patients with a first episode of a symptomatic pneumothorax admitted to
the ER of the hospital (spontaneous or traumatic) or
2.patients with an asymptomatic pneumothorax with a size of >= 20 % as
estimated by Light*s formula.
3.age >= 18 and < 85 years.
4.smoking is tolerated.
1.re-pneumothorax
2.lung fibrosis
3.pregnant women
4.comorbidity limiting decision making (psychiatric disease, alcohol or
drug abuse
5.COPD patients.
6.Marfan syndrome.
7.lung cancer patients.
8.tension pneumothorax.
9.prior randomisation
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>1.The duration of LOS of each technique.</p><br>
- Secondary Outcome Measures
Name Time Method <p>1.The success rate of each technique:<br /><br><br /><br>1. immediate: see below<br /><br>2. two weeks: continous expansion<br /><br>3. one year: no recurrence of the pneumothorax.<br /><br><br /><br><br /><br>Conventional chest tube drainage; complete expansion of the lung,<br /><br>counteraction of the air leak and removal of the drain within 72 hours<br /><br>(immediate).<br /><br><br /><br>Manual aspiration: complete expansion and discharge within 24 hours<br /><br>(immediate).<br /><br><br /><br></p><br>