Status:
COMPLETED
Virtual Reality in Laryngology
Lead Sponsor:
Weill Medical College of Cornell University
Conditions:
Pain Management During Office Laryngeal Procedures
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
The purpose of this study is to compare patient's pain and anxiety undergoing laryngeal procedures and esophageal manometry while wearing a VR headset to standard of care. It is hypothesized that pati...
Detailed Description
This is a prospective randomized controlled trial, comparing patients' pain and anxiety experience while wearing a VR headset and receiving standard analgesia during In-office aerodigestive procedures...
Eligibility Criteria
Inclusion
- Adult patients (18 or older)
- Patients scheduled for IOAEP, including laryngeal biopsies, percutaneous injection laryngoplasty, KTP ablation of hemorrhagic polyps and respiratory papilloma, and transnasal esophagoscopy (TNE), and esophageal manometry.
Exclusion
- Patients under 18 years of age
- Patients unable to consent
- Non-English-speaking patients
- Patients who have undergone prior IOAEP
- Patients who have used any psychotropic or analgesic medication within the last 24 hours due to the possible confounding effect on pain or anxiety perception
- Patients with motion sickness or uncorrected visual impairment (legal blindness)
- Patients with past medical history of seizures or visual abnormalities
Key Trial Info
Start Date :
February 14 2022
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
August 8 2022
Estimated Enrollment :
40 Patients enrolled
Trial Details
Trial ID
NCT05218967
Start Date
February 14 2022
End Date
August 8 2022
Last Update
February 22 2024
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
Weill Cornell Medicine
New York, New York, United States, 10021