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
NA
43 participants
INTERVENTIONAL
2020-06-17
2021-06-17
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
OTHER
NONE
Study Groups
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Electronic Intervention
Individualized opioid taper and safety recommendations will be communicated to prescribers via an electronic medical record encrypted message.
opioid prescribing
Individualized taper and safety recommendations will be communicated to prescribers via an electronic medical record encrypted message.
Interventions
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opioid prescribing
Individualized taper and safety recommendations will be communicated to prescribers via an electronic medical record encrypted message.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
65 Years
ALL
No
Sponsors
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Stanford University
OTHER
Responsible Party
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Huiqiong Deng
Clinical Assistant Professor
Principal Investigators
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Huiqiong Deng, MD, PHD
Role: PRINCIPAL_INVESTIGATOR
Stanford Univeristy
Locations
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Stanford University
Stanford, California, United States
Countries
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Other Identifiers
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IRB-54148
Identifier Type: -
Identifier Source: org_study_id