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Enrolling by invitation NCT04893278

Virtual Reality in Electrophysiology Laboratory (EP)

— Observational PVC - Premature Ventricular Complex Ablation

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Virtual reality.
Who it may be relevant to
Registry conditions: PVC - Premature Ventricular Complex, Ablation. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Use of Virtual Reality as An Adjunct for Anesthesia During Procedures in the Electrophysiology Laboratory: A Pilot and Feasibility Study

Overview

The purpose of this study is to evaluate the use of virtual reality (VR) technology as adjunct to routine anesthesia care for patients undergoing electrophysiology (EP) procedures.

Interventions

  • Other Virtual reality
    Use of Virtual reality goggles during procedure

Primary outcome measures

  • Virtual reality as distractor [Time frame: Up to 2hours]
Secondary outcome measures (2)
  • Impact of virtual reality use on pharmacological therapy [Time frame: Up to 2 hours]
  • Impact of virtual reality on electrophysilogy procedure [Time frame: Up to 2 hours]

Eligibility criteria

Inclusion criteria

  • Age ≥ 18 years old.
  • Patients scheduled for electrophysiology procedure with MAC.
  • Subject willing to participate and able to provide informed consent.

Exclusion criteria

  • Age < 18 years old.
  • History of motion sickness or blindness.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Case-only

Study locations

United States · 1 center
  • Mayo Clinic in Florida — Jacksonville

Identifiers

NCT: NCT04893278 · 21-002644

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗