This is a prospective, randomized, double-blind, Phase II, clinical trial to evaluate sameridine hydrochloride, a new type of compound with both the local anesthetic and analgesic properties. The study involves spinal adminstration of sameridine or lidocaine as the anesthetic for patients undergoing inguinal herniorraphy. As part of this study, patients will be required to stay in the hospital for 24 hours following surgery. The GCRC is required so blood samples may be drawn and hoursly data collected (vital signs) and pain scores (VAS scores).

Project Start
1997-02-04
Project End
1997-11-30
Budget Start
1996-10-01
Budget End
1997-09-30
Support Year
35
Fiscal Year
1997
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Type
DUNS #
073133571
City
San Francisco
State
CA
Country
United States
Zip Code
94143
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