Actively Recruiting

Phase Not Applicable
All Genders
NCT06247800

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

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Participants undergoing intercostal chest drain (ICC) insertion
  • Participants who can understand and provide consent
Not Eligible

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

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Trial Site Locations

Total: 1 location

1

National University of Malaysia

Kuala Lumpur, Kuala Lumpur, Malaysia, 56000

Actively Recruiting

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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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