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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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19 April 2022 |
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Main ID: |
NCT03106129 |
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Date of registration:
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04/04/2017 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Opioid Requirements Post Discharge of Patients Having Total Knee Arthroplasty (TKA)
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Scientific title:
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Opioid Requirements Post Discharge of Patients Having Total Knee Arthroplasty (TKA) |
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Date of first enrolment:
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February 9, 2017 |
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Target sample size:
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200 |
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Recruitment status: |
Active, not recruiting |
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URL:
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https://clinicaltrials.gov/show/NCT03106129 |
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Study type:
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Observational |
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Study design:
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Phase:
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Countries of recruitment
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Canada
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Contacts
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Name:
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Imad Awad, MBChB |
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Address:
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Telephone:
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Email:
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Affiliation:
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Sunnybrook Health Sciences Centre |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- 18 years or older
- Having an elective total knee replacement done at Sunnybrook Holland Orthopaedic and
Arthritic Centre.
- All participants must speak English and have no communication barriers.
Exclusion Criteria:
- If you are taking >10mg morphine equivalents per day
- Deemed incompetent to be able to self prescribe opioids.
Age minimum:
18 Years
Age maximum:
N/A
Gender:
All
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Health Condition(s) or Problem(s) studied
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Rehabilitation
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Pain
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Knee Arthropathy
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Opioid Use
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Primary Outcome(s)
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The amount of opioid analgesics used and the number remaining
[Time Frame: 6 weeks after surgery]
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Secondary Outcome(s)
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The amount of non-opioid analgesics consumed
[Time Frame: 6 weeks after surgery]
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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