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Local infiltration analgesia for Shoulder Osteoarthritis
Study Summary
This trial will compare the efficacy of local infiltration analgesia to interscalene block in shoulder arthroplasty patients in regards to pain scores, opiate consumption, and complication rates.
- Shoulder Osteoarthritis
- Cuff Tear Arthropathy
- Rotator Cuff Tears
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Trial Design
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Who is running the clinical trial?
Frequently Asked Questions
What are the end goals of this particular research endeavor?
"The primary goal of this medical research, to be evaluated between 4 hours and 2 weeks postop, is evaluating opioid use. Ancillary goals encompass the duration of surgery, any potential postoperative issues (medical complications, nerve damage, dislocations etc.), as well as intra-surgical difficulties (fractures/vascular injuries associated with general anaesthesia)."
How many participants are taking part in this experimental research project?
"Affirmative. Clinicaltrials.gov records reveal that, as of December 1st 2021, this trial is still actively enrolling participants. It was first announced on August 15th 2020 and the aim is to recruit 74 patients from a single site."
Does the current recruitment period for this research study still allow for new participants?
"This investigation, which was initially announced on August 15th 2020 is currently recruiting participants. The trial's information has been updated most recently on December 1st 2021 according to clinicaltrials.gov."
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