Actively Recruiting
Novel Endoscopic Bite Block
Led by University of Pennsylvania · Updated on 2026-01-16
50
Participants Needed
1
Research Sites
49 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This feasibility study aims to assess the safety and effectiveness of the Novel Endoscopic Bite Block. The device will be utilized in subjects undergoing routine outpatient upper endoscopy. The investigator hypothesizes that its innovative design will reduce complications associated with bite block positioning, thereby improving procedural efficiency and patient safety.
CONDITIONS
Official Title
Novel Endoscopic Bite Block
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Signed and dated informed consent form
- Willingness to comply with all study procedures and availability for the study duration
- Male or female, 21 years of age or older
- Considered appropriate for scheduled upper endoscopy by endoscopists and anesthesia staff
You will not qualify if you...
- Known allergic reactions to thermoplastic polyurethane (TPU), used in the bite block
- Any medical condition that makes the subject ineligible according to the principal investigator's opinion
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Penn Medicine Princeton Health
Plainsboro, New Jersey, United States, 08536
Actively Recruiting
Research Team
M
Monica Saumoy, MD, MS
CONTACT
S
Sheryl Smolensky, RN, MSN, OCN
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
DEVICE_FEASIBILITY
Number of Arms
1
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