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*A prospective, randomised trial in pneumothorax therapy: manual aspiration versus conventional chest tube drainage.*

Recruiting
Conditions
lung rupture
pneumothorax
10035597
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
Inclusion Criteria

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.

Exclusion Criteria

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
NameTimeMethod
<p>1.The duration of LOS of each technique.</p><br>
Secondary Outcome Measures
NameTimeMethod
<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>
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