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
About this trial
This is an interventional prevention trial for Bite Block focused on measuring bite block, transesophageal echocardiography
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
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
NCT ID
NCT04236297
First Posted
January 10, 2020
Last Updated
April 9, 2022
Sponsor
University of Washington
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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