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Clinical Trial Summary

This study is a prospective, randomized trial. Our study aims to study the effects of perioperative patient education about compartment syndrome on patients' perception of their own pain, amount of opioid medication utilization, and rate of diagnosis of compartment syndrome.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03359031
Study type Interventional
Source Rothman Institute Orthopaedics
Contact
Status Enrolling by invitation
Phase N/A
Start date November 13, 2017
Completion date November 2018

See also
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Recruiting NCT06050499 - Chemical Analysis of Limb Microfluidics
Recruiting NCT04806555 - Diagnostic Value of Compression Ultrasound to Detect Acute Compartment Syndrome After Lower Limb Revascularisation N/A
Not yet recruiting NCT06079255 - Ischemia Detection During Development of Acute Compartment Syndrome
Recruiting NCT05466539 - Chronic Exertional Compartment Syndrome (CECS) Treated With Abobotulinumtoxin A Phase 4