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Suction Versus Water Seal for Initial Treatment of Traumatic Pneumothorax Trial

Not Applicable
Recruiting
Conditions
Pneumothorax
Trauma
Registration Number
NCT06688734
Lead Sponsor
Vanderbilt University Medical Center
Brief Summary

The goal of this clinical trial is to compare the effect of placing chest tubes to water seal versus suction initially, in patients with traumatic pneumothoraces, on overall chest tube duration.

The main question it aims to answer is:

* Does placing chest tubes to water seal initially results in a shorter chest tube duration, without an increase in complications?

Alternating each month, patients' chest tubes will either be placed to water seal or to suction initially. All other management decisions related to the chest tube will be left to the providers.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
150
Inclusion Criteria
  • admitted to the trauma surgery service
  • pneumothorax requiring a chest tube
Exclusion Criteria
  • less than 18 years olf
  • pregnant
  • prisoner
  • greater than 300cc of hemothorax on CT
  • chest tube placed prior to CT scan

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Chest tube durationThrough study completion, an average of 1 year

Duration of the initial chest tube, measured in hours

Secondary Outcome Measures
NameTimeMethod
Change from water seal to suctionThrough study completion, an average of 1 year

Yes/No

Additional chest tube placement on affected sideThrough study completion, an average of 1 year

Yes/no

Pneumothorax reaccumulation with chest tube to water sealThrough study completion, an average of 1 year

Yes/no Yes if growth of pneumothorax on chest x-ray with tube to water seal

Replacement of chest tubeThrough study completion, an average of 1 year

Yes/no Yes if chest tube removed and then a new one is place on the same side at a later time

Pneumothorax reaccumulation after chest tube removalThrough study completion, an average of 1 year

Yes/no Yes if pneumothorax grows on chest x-ray after chest tube removal

Hypoxic eventsThrough study completion, an average of 1 year

Yes/no Yes if \<90% O2 saturation is recorded in chart

EmpyemaThrough study completion, an average of 1 year

Yes/no Yes if clinically diagnosed by provider based off of imaging, operative findings, clinical picture, culture results, or operative findings

PneumoniaThrough study completion, an average of 1 year

Yes/no Yes if clinically diagnosed and treated for pneumonia

Retained hemothoraxThrough study completion, an average of 1 year

Yes/no Yes if \>300cc hemothorax seen on CT scan after chest tube placement

TPA administrationThrough study completion, an average of 1 year

Yes/no Yes if any TPA administered to the affected side of the chest

Chest tube site, skin and soft tissue infectionThrough study completion, an average of 1 year

Yes/no Yes if skin and soft tissue infection treated with incision and drainage, or antibiotics

Video-assisted thoracoscopic surgeryThrough study completion, an average of 1 year

Yes/no Yes if receives video-assisted thoracoscopic surgery on the affected side during initial admission

Acute respiratory failure requiring intubationThrough study completion, an average of 1 year

Yes/no Yes if intubated for hypoxia or hypercapnea during hospital stay

Unplanned ICU admissionThrough study completion, an average of 1 year

Yes/no Yes if admitted to ICU unexpectedly, for clinical deterioration

30-day mortalityThrough study completion, an average of 1 year

Yes/no Yes if died within 30 days of initial presentation

Length of hospital stayThrough study completion, an average of 1 year

Integer, measured in days, length of initial hospital stay

30-day readmissionThrough study completion, an average of 1 year

Yes/no Yes if readmitted within 30 days of discharge

Thoracic intervention during readmissionThrough study completion, an average of 1 year

Yes/no Yes if readmitted and receives chest tube, video-assisted thoracoscopic surgery, or thoracotomy on the affected side

Trial Locations

Locations (1)

Vanderbilt University Medical Center

🇺🇸

Nashville, Tennessee, United States

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