RecruitingACTRN12624001301550

Analogue versus Digital Intervention in Chest Trauma (ADICT): A prospective randomized control trial on the efficacy of digital thoracostomy drain versus the analogue counterpart following major thoracic trauma

Analogue versus Digital Intervention in Chest Trauma (ADICT): A prospective randomized control trial on the efficacy of digital thoracostomy drain versus the analogue counterpart following major thoracic trauma in participants 16 years or older


Sponsor

Royal Melbourne Hospital

Enrollment

262 participants

Start Date

Feb 5, 2025

Study Type

Interventional

Conditions

Summary

Despite the technological innovation and potential for improved care, the use of digital drainage systems has not been well evaluated for trauma care. Decreasing the length of time that patients have an invasive intrathoracic device is expected to impact length of stay (LOS) in hospital, intensive care, and risk of adverse outcomes. This study aims to investigate the efficacy of digital thoracostomy drain in the setting of major thoracic trauma and we hypothesize that it could reduce the length of inter-costal catheterisation (ICC) time compared to the analogue counterpart.


Eligibility

Sex: Both males and femalesMin Age: 16 Yearss

Plain Language Summary

Simplified for easier understanding

When someone sustains a serious chest injury, they often need a drain inserted between the ribs to remove fluid or air from around the lungs — a procedure called intercostal catheter placement. Traditionally, these drains use analogue (non-digital) water-seal devices to monitor drainage. Newer digital systems can more precisely measure and display what is draining, which may allow doctors to remove the drain sooner and reduce the time patients spend in hospital. This randomised trial compares digital drain systems to standard analogue systems in patients admitted to the Royal Melbourne Hospital with major chest trauma. The main goal is to find out whether the digital system reduces how long patients need the drain in place, and whether this translates into shorter hospital stays. You may be eligible if you are 16 or older and have sustained a traumatic chest injury that requires a drain to be inserted. People who had a drain inserted before reaching hospital, those with extremely large volumes of blood in the chest (massive haemothorax), or those who required emergency chest surgery in the department are not eligible.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

digital chest drain system for use in traumatic pneumonia/haemthorax. This drain will be connected directly to the intercostal catheter (ICC) in the same way as the current analogue drain is. Members

digital chest drain system for use in traumatic pneumonia/haemthorax. This drain will be connected directly to the intercostal catheter (ICC) in the same way as the current analogue drain is. Members of the trauma team (RNs or doctors) connect this train as part of the procedure when inserting an ICC. The duration of the ICC insertion / drain is dependent upon the lung reinflating, but is usually 2-3 days. Review of electronic medical records will be used to determine this. All data will be available from the EMR. Although the digital drain offers further data (e.g. air leak) it will not be used as part of the study as comparable data can not be collected for analogue drains.


Locations(1)

Royal Melbourne Hospital - City campus - Parkville

VIC, Australia

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