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Clinical Trial Summary

Primary aim:

1. To compare the nerve stimulation vs. anatomic techniques of paravertebral block of T11-L1 in providing surgical anesthesia for patients undergoing inguinal hernia repair.

Secondary aims:

1. Compare VAS pain scores in the two groups of patients over the first 24 hours.

2. Compare opioid intake over the first 24 hours in the two groups of patients.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Supportive Care


Related Conditions & MeSH terms


NCT number NCT00587704
Study type Interventional
Source Mayo Clinic
Contact
Status Completed
Phase N/A
Start date July 2007
Completion date May 2009

See also
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