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

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

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON30187
Enrollment
114
Registered
2006-08-29
Start date
2007-06-01
Completion date
Unknown
Last updated
2024-06-18

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

Conditions

lung rupture pneumothorax

Interventions

Conventional chest tube drainage: After skin desinfection and field preparation, a pneumocath catheter with a diameter of 2,7 mm will be introduced in the second or third intercostal space in the a

Sponsors

Isala Klinieken
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

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

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frame
1.The duration of LOS of each technique.

Secondary

MeasureTime frame
1.The success rate of each technique: 1. immediate: see below 2. two weeks: continous expansion 3. one year: no recurrence of the pneumothorax. Conventional chest tube drainage; complete expansion of the lung, counteraction of the air leak and removal of the drain within 72 hours (immediate). Manual aspiration: complete expansion and discharge within 24 hours (immediate).

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)