Florida Orthopaedic Institute
Tampa, Florida, 33736, United States
NCT Number: NCT05240755
This study is a prospective, randomized, nonblinded trial to evaluate the effectiveness of Cannabidiol (CBD) oil on post-operative pain control compared to opioid medications.
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Notify Me18 year and older
All sexes
Interventional
Early Phase 1
Tampa, Florida, 33736, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Subjects will self-administer CBD sublingually.
Time frame: 30 days post-operatively
Numerical Pain Scale (NRS): 0 being no pain, 10 being the worst pain imaginable. Higher scores are worse outcomes.
Time frame: 30 days preoperatively leading up to surgery then 30 days postoperatively as well. Outcomes will be collected from surgery to 6 weeks postoperatively.
Insomnia Severity Index
Foundation for Orthopaedic Research and Education
Other
Acronym: CBDS
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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