Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
100 participants
OBSERVATIONAL
2018-03-01
2022-12-31
Brief Summary
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Detailed Description
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1. pain levels post-surgery as recorded by Likert-type and Gracely scales
2. quality of life(QOL) outcomes for lifestyle and oral function
3. number of opioid doses taken by subject-patients
4. number of NSAID and acetaminophen doses taken by subject-patients.
Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Interventions
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third molar surgery
The patient is asked to complete the diary each post-surgery day for 14 days. Recovery is organized into three QOL domains: lifestyle, oral function, and pain.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
35 Years
ALL
Yes
Sponsors
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University of North Carolina, Chapel Hill
OTHER
Responsible Party
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Principal Investigators
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Glenn Reside, DMD
Role: PRINCIPAL_INVESTIGATOR
UNC oral and maxillofacial surgery
Locations
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University of North Carolina School of Dentistry
Chapel Hill, North Carolina, United States
Countries
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Other Identifiers
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18-0047
Identifier Type: -
Identifier Source: org_study_id
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