Effects of an External Oral Irrigation Device on Patients With Dry Mouth
NCT ID: NCT04901507
Last Updated: 2023-07-24
Study Results
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View full resultsBasic Information
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COMPLETED
NA
16 participants
INTERVENTIONAL
2021-05-20
2022-04-28
Brief Summary
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Detailed Description
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In this study, participants will be asked to:
1. Visit the dental school clinic two (2) times for study visits.
2. Wear the oral irrigation device as directed by the investigator.
3. Keep notes at home.
4. Answer survey questions during both dental visits about dry mouth symptoms.
5. Give permission for the researchers to collect information about medications or health conditions that contribute to dry mouth from participant's medical records.
Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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The Voutia System
The Voutia System oral irrigation device
The Voutia System
Participants will wear the Voutia System oral irrigation device continuously through the day and night, removing for cleaning and if otherwise necessary, but not for time extending beyond six-eight hours.
Interventions
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The Voutia System
Participants will wear the Voutia System oral irrigation device continuously through the day and night, removing for cleaning and if otherwise necessary, but not for time extending beyond six-eight hours.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Children
* Patient with limited English proficiency
18 Years
ALL
No
Sponsors
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Voutia
INDUSTRY
Virginia Commonwealth University
OTHER
Responsible Party
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Principal Investigators
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Susie Goolsby, DDS, MSHA
Role: PRINCIPAL_INVESTIGATOR
Virginia Commonwealth University
Locations
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Virginia Commonwealth University
Richmond, Virginia, United States
Countries
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Provided Documents
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Document Type: Study Protocol
Document Type: Statistical Analysis Plan
Document Type: Informed Consent Form
Other Identifiers
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HM20021188
Identifier Type: -
Identifier Source: org_study_id
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