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Evaluation of Modified Bite-Block for Invasive Imaging Procedures

Primary Purpose

Bite Block

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
bite block
Sponsored by
University of Washington
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Bite Block focused on measuring bite block, transesophageal echocardiography

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 18 years of age or older
  • Undergoing stand-alone transesophageal echocardiography exam under sedation or general anesthesia
  • Undergoing procedure that requires transesophageal echocardiography exam during the procedure under general anesthesia
  • Cardiology and cardiac anesthesiology echocardiographers performing transesophageal echocardiography exam who wish to participate

Exclusion Criteria:

  • Less than 18 years of age
  • Any procedure that does not require transesophageal echocardiography exam during the procedure

Sites / Locations

  • University of Washington

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Modified Bite Block

Arm Description

Patients undergoing transesophageal echocardiogram under sedation or general anesthesia during which a modified bite block is used

Outcomes

Primary Outcome Measures

Oral injury
Number of participants with oral injury (dental injury, lacerations/bruises on gums and lips) which will be determined by examination

Secondary Outcome Measures

Dislodgment
Number of participants with bite block dislodgment which will be determined by provider questionnaire
Provider satisfaction
Number of providers that would use standard or redesigned bite block again

Full Information

First Posted
January 10, 2020
Last Updated
April 9, 2022
Sponsor
University of Washington
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1. Study Identification

Unique Protocol Identification Number
NCT04236297
Brief Title
Evaluation of Modified Bite-Block for Invasive Imaging Procedures
Official Title
Evaluation of Modified Bite-Block vs Standard Bite Block for Invasive Imaging Procedures
Study Type
Interventional

2. Study Status

Record Verification Date
April 2022
Overall Recruitment Status
Completed
Study Start Date
August 22, 2019 (Actual)
Primary Completion Date
August 30, 2020 (Actual)
Study Completion Date
December 31, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Washington

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to compare a modified bite block with standard bite block during transesophageal echocardiography procedures in patients who are either sedated or under general anesthesia. These dental protector devices are class I devices which are exempt from the FDA 510(k) premarket notification requirements.
Detailed Description
Bite block is a single-use medical device used to keep the mouth open during invasive imaging procedures and prevent the patient from biting the imaging probe. The purpose of this study is to compare a modified bite block with standard bite block during transesophageal echocardiography exam procedures in patients who are either sedated or under general anesthesia. The commercially available bite blocks are almost exclusively made of hard plastic that does not conform well to the patient's mouth with additional protrusions used to secure the bite block in place that have the potential to cause patient injury. Hard plastic is used to prevent patient from biting down on the imaging probe while side protrusions are used to strap the bite block down to prevent dislodgment. Modified bite block is made of softer material with improved mouth fit and no need for strapping the bite block to keep it in place. Softer material is more comfortable while the designs mimics mouth guard used in dentistry to protect patient's teeth and keep the bite block in place while sleeping. The specific aims of this project include: assessment of patient comfort during invasive imaging procedure assessment of provider satisfaction with the bite block assessment of patient lip/gum/teeth injury after bite block use assessment of imaging probe damage after procedure assessment of bite block's ability to stay in place during procedure

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bite Block
Keywords
bite block, transesophageal echocardiography

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
50 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Modified Bite Block
Arm Type
Other
Arm Description
Patients undergoing transesophageal echocardiogram under sedation or general anesthesia during which a modified bite block is used
Intervention Type
Device
Intervention Name(s)
bite block
Intervention Description
Physicians performing transesophageal echocardiogram in patients under sedation or general anesthesia will use either standard or modified bite block.
Primary Outcome Measure Information:
Title
Oral injury
Description
Number of participants with oral injury (dental injury, lacerations/bruises on gums and lips) which will be determined by examination
Time Frame
Within 24 hours
Secondary Outcome Measure Information:
Title
Dislodgment
Description
Number of participants with bite block dislodgment which will be determined by provider questionnaire
Time Frame
Within 24 hours
Title
Provider satisfaction
Description
Number of providers that would use standard or redesigned bite block again
Time Frame
Within 24 hours

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 18 years of age or older Undergoing stand-alone transesophageal echocardiography exam under sedation or general anesthesia Undergoing procedure that requires transesophageal echocardiography exam during the procedure under general anesthesia Cardiology and cardiac anesthesiology echocardiographers performing transesophageal echocardiography exam who wish to participate Exclusion Criteria: Less than 18 years of age Any procedure that does not require transesophageal echocardiography exam during the procedure
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Srdjan Jelacic, MD
Organizational Affiliation
University of Washington
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Washington
City
Seattle
State/Province
Washington
ZIP/Postal Code
98195
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Evaluation of Modified Bite-Block for Invasive Imaging Procedures

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