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Clinical Trial Summary

The goal of this project is to perform a randomized, double-blinded study investigating postoperative pain after arthroscopic rotator cuff using hyperosmolar saline as opposed to lactated ringer's solution (normal osmolarity) as arthroscopy irrigation solutions. Hyperosmolar saline is an irrigation solution with a higher concentration of solutes that will be used intraoperatively to washout the surgical field. It will be used in place of lactated ringer's solution, which has an osmolarity comparable to that of normal saline. This study will help determine whether or not postoperative pain from rotator cuff repair can be mitigated by altering the osmolarity of the intraoperative irrigation solution. This knowledge is significant because the postoperative pain can be intense, so much so that patients may depend on narcotics for pain relief. Consequently, this study may provide benefit by helping to find new ways to minimize the need for narcotics. The main hypothesis of this is study is that hyperosmolar saline will reduce perceived pain and narcotic use in the postoperative period.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03738735
Study type Interventional
Source Rothman Institute Orthopaedics
Contact Liam Kane, BS
Phone 2673393593
Email Liam.Kane@rothmanortho.com
Status Not yet recruiting
Phase Phase 4
Start date January 2019
Completion date June 2020

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