Actively Recruiting
Virtual Reality: Distraction During Small Bore Intercostal Chest Drain Insertion
Led by National University of Malaysia · Updated on 2025-11-19
80
Participants Needed
1
Research Sites
151 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Virtual Reality: Distraction During Small Bore Intercostal Chest Drain Insertion
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Participants undergoing intercostal chest drain (ICC) insertion
- Participants who can understand and provide consent
You will not qualify if you...
- Participants unable to understand or give consent
- Ventilated patients
- Participants uncomfortable wearing the VR device
- Participants unable to communicate due to illiteracy, hearing impairment, muteness, blindness, or memory issues
- Participants with craniofacial deformities
- Participants taking sedative medications
- Traumatic or post motor vehicular accident patients
- Participants undergoing indwelling pleural catheter insertion
- Participants with anxiety disorders
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
National University of Malaysia
Kuala Lumpur, Kuala Lumpur, Malaysia, 56000
Actively Recruiting
Research Team
M
Mohamed Faisal Abdul Hamid, MBBS (IIUM)
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
2
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