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
77 participants
OBSERVATIONAL
2016-09-01
2017-03-01
Brief Summary
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The primary objective of the study is to compare patients' reported pain and narcotic use following meniscectomy, and determine if NSAIDs can provide adequate pain relief.
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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Patients with pain following knee arthroscopic meniscectomy
Ibuprofen 600 mg
Ibuprofen 600 mg to be taken every 8 hours (TID) as needed (PRN
standard oxycodone/acetaminophen
Interventions
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Ibuprofen 600 mg
Ibuprofen 600 mg to be taken every 8 hours (TID) as needed (PRN
standard oxycodone/acetaminophen
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* ASA class I-II
* Patients scheduled for meniscectomy
Exclusion Criteria
* Legally incompetent or mentally impaired (e.g. minors, Alzheimer's subjects, dementia, etc.)
* Younger than 18 years of age or older than 65
* Any patient considered a vulnerable subject
* Patients on pain medication prior to surgery
18 Years
ALL
Yes
Sponsors
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NYU Langone Health
OTHER
Responsible Party
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Principal Investigators
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Kirk Campbell, MD
Role: PRINCIPAL_INVESTIGATOR
New York University Medical School
Locations
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New York University School of Medicine
New York, New York, United States
Countries
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Other Identifiers
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16-01645
Identifier Type: -
Identifier Source: org_study_id
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