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Clinical Trial Summary

Over 600,000 hysterectomies are performed annually in the United States. Despite increasing use of less invasive approaches, the majority of hysterectomies are still performed via traditional laparotomy, which can be associated with generally slower recovery and longer lengths of post-operative hospitalization. Rapid Recovery Protocols (RRP) seek to optimize post-surgical morbidity outcomes by returning a patient to normal physiology as quickly as possible following surgery.


Clinical Trial Description

Subjects will be randomly assigned to one of two groups: Rapid recovery protocol (regional anesthesia, pain control options with emphasis on nonsteroidal anti-inflammatory drugs (NSAIDS) over narcotic pain medications, early ambulation, and early enteral feeding) or standard of care (traditional laparatomy and supportive care). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01705288
Study type Interventional
Source Masonic Cancer Center, University of Minnesota
Contact
Status Completed
Phase Early Phase 1
Start date January 1, 2013
Completion date August 24, 2016

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