Implementing Virtual Reality (VR) to Reduce Sedation

Recruiting N/A Interventional Study
Sedative During Endoscopy
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part.
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At a Glance
Age
21 – 65
Sex
Any
Study type
Interventional
Purpose
Supportive Care
Participants needed
10 (estimated)
Sponsor
NYU Langone Health · Other
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About This Trial
The study is a prospective pilot patients aged 21 to 65 undergoing screening colonoscopy or diagnostic upper endoscopy. Patients are administered minimal sedation (2 mg of Versed and 25 mg of Fentanyl) and are given Virtual Reality (VR) goggles to wear for the duration of the procedure. The purpose of this study is to assess the feasibility, effect, and safety of using VR goggles during endoscopic…
Trial Locations
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Eligibility Criteria
INTERVENTION GROUP Inclusion Criteria: * Undergoing screening colonoscopy or diagnostic upper endoscopy for GERD or dyspepsia at NYU Langone Brooklyn Hospital * Aged 21 to 65 Exclusion Criteria: * Visual impairments such as blindness which would impair them from watching the entertainment videos…
Contacts

Maysaa El Zoghbi, MD

216-835-7626

Maysaa.ElZoghbi@nyulangone.org

CONTACT

Gregory Faulx

216-213-7413

gregory.faulx@nyulangone.org

CONTACT