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Clinical Trial Summary

The purpose of this study is that an adductor canal nerve block (putting numbing medicine near the nerve) has been shown to produce excellent pain relief with less pain medication use after knee replacement surgery.The investigators will be comparing the amount of pain relief following knee replacement surgery when you have a nerve block in place. There will be approximately 66 subjects participating in this study. After surgery subjects will receive numbing medication every 6 hours for 48 hours. Subjects will also receive a morphine PCA (patient controlled analgesia) after surgery and pain medication by mouth every 4 hours around the clock with the option to receive more pain medication if needed. Subjects will participate in the study up to 3 days.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01939379
Study type Interventional
Source Loma Linda University
Contact
Status Withdrawn
Phase N/A
Start date September 2013
Completion date July 25, 2017

See also
  Status Clinical Trial Phase
Completed NCT02244619 - PO vs. IV Acetaminophen Given Perioperatively for 24 hr Post-op Pain Control Following Total Hip or Knee Replacement Phase 4
Not yet recruiting NCT02123979 - Study to Assess Dopamine Receptor Modulation With Rotigotine to Enhance Morphine Analgesia in the Dental Model Phase 2