Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
Shoulder Pain
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentIntervention Model Description: Participants (stratified into five surgical categories) will be randomized into one of the three study arms.Masking: Triple (Participant, Investigator, Outcomes Assessor)Masking Description: participants will be masked to the aspect of post-operative pain management being manipulated in this study; investigator and outcomes assessor will be masked to randomization (group assignment) of participantsPrimary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 90 years
Gender
Both males and females

Description

There is currently very limited information in the literature regarding postoperative pain medication consumption following orthopedic shoulder surgery. To fill this knowledge gap, this study will evaluate overall opioid consumption in morphine milligram equivalents and non-narcotic analgesic use fo...

There is currently very limited information in the literature regarding postoperative pain medication consumption following orthopedic shoulder surgery. To fill this knowledge gap, this study will evaluate overall opioid consumption in morphine milligram equivalents and non-narcotic analgesic use following surgical treatment for shoulder pathology.

Tracking Information

NCT #
NCT04622839
Collaborators
American Shoulder and Elbow Surgeons
Investigators
Principal Investigator: Umasuthan Srikumaran, M.D. Johns Hopkins Orthopedics