American University of Beirut Medical Center
Beirut, Lebanon
NCT Number: NCT03732456
A prospective observational study conducted at the American University of Beirut Medical center that targets patients undergoing shoulder surgeries. It is conducted to to prospectively collect patient, surgery and anesthesia-related variables and perform correlation studies with postoperative pain severity, patients' satisfaction and analgesic consumption following shoulder surgery.
In addition, identifying predictors for postoperative pain will contribute to adjust pain management protocols as per surgical and patients' factors.
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Notify Me18 year and older
All sexes
Observational
Beirut, Lebanon
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Usual care surgery (shoulder arthroscopy) and post-operative pain management protocol
Time frame: 24 hours, 3 days and one week after surgery
Asses the change in pain intensity after the surgery using the NRS pain score (0-10)
Time frame: 24 hours, 3 days and one week after surgery
Asses the change in satisfaction with the pain management protocol using the NRS satisfaction score (0-10)
Time frame: Over one week
Analgesic consumption over one week after the surgery
Time frame: One week after surgery
The QuickDASH questionnaire includes questions about the symptoms and ability to do certain activities
American University of Beirut Medical Center
Other
Predictors of Post-operative Pain in Shoulder Surgery, a Prospective Observational Study
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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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