Novel Endoscopic Bite Block

Completed · Not applicable

Conditions studied: Gastric Disease

In brief

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.

Key facts

Study ID

NCT06958250

Run by

University of Pennsylvania

People needed

45

Starts

2025-12-22

Expected to finish

2026-05-28

Last updated by the study team

2026-06-02

Who can join

Age: 21 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Provision of a signed and dated Informed Consent Form (ICF).
• Stated willingness to comply with all study procedures and availability for the duration of the study.
• Male or female, ≥21 years of age.
• Deemed appropriate for scheduled upper endoscopy by endoscopists and anesthesia staff.

You may not qualify if…

• Known allergic reactions to thermoplastic polyurethane (TPU), the component used in the manufacturing of the Flexible Endoscopic Bite Block.
• Any medical condition that, in the opinion of the PI, makes the subject ineligible to participate in the clinical trial.

Where it is running

• Penn Medicine Princeton Health — Plainsboro, New Jersey, United States

Full record on ClinicalTrials.gov

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