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Study identifier: NCT06247800 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Virtual Reality: Distraction During Small Bore Intercostal Chest Drain Insertion

Condition: Pleural Effusion  ·  Sponsor: National University of Malaysia

PhaseNA
Planned participants80
Who can joinAll sexes, N/A to no upper limit
Healthy volunteersNo

About this study

Intercostal chest drain (ICC) insertion is a common procedure done worldwide to treat and diagnose pleural disease. It is used to evacuate fluid, blood, or air in the cavity from a myriad of causes namely pleural effusions of different etiologies, empyema, hemothorax, chylothorax and pneumothorax. It also functions as a route for antibiotics, pleurodesis and fibrinolytics. Hippocrates, whose practiced medicine 2,400 years ago, is often credited with being the first to insert a metal tube into the pleural region to drain fluid. It wasn't until the 19th century that a closed drainage system was properly documented in the literature, although open drainage remained to be the norm for quite some time. In the past, large-bore tubes (24-32 F) were recommended in nearly all circumstances and were inserted using a blunt dissection technique. However, during the past two decades, small-bore catheters have become increasingly popular. They were first used to drain abdominal collections and have now been adopted for use in draining the pleural cavity utilizing the needle and guide wire Seldinger procedure, typically with radiological guidance. In addition to that, Seldinger technique allow us to insert the catheter at lower intercostals spaces without injury to the diaphragm or abdominal organs, thereby ensuring patient safety.

This description comes directly from the study's public registry record.

Talk to the study team

Mohamed Faisal Abdul Hamid, MBBS (IIUM)  ·  0391455555  ·  faisal.hamid@ppukm.ukm.edu.my

Always discuss trial participation with your own doctor first.

Locations (1)

National University of MalaysiaKuala Lumpur, Kuala Lumpur, MalaysiaRecruiting

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Source record: clinicaltrials.gov/study/NCT06247800