drugset / Trial / NCT00913003

Analgesic Effect of Perioperative Systemic Lidocaine in Patients Undergoing Unilateral Mastectomy Surgery

NCT00913003 ↗

Phase 4 Terminated 22 enrolled Northwestern University
RandomizedParallel-groupTriple-blindPrevention

Summary

The aim of this study is to determine if perioperative systemic lidocaine administration will decrease the amount of opioid analgesics required in women undergoing mastectomy surgery. In addition, patients receiving systemic lidocaine will have a lower incidence of post-mastectomy pain syndrome. This study will have 2 groups. Participants will be randomized into one of each group. The first group will be administered the drug lidocaine prior to surgery and the second group Group B will be administered saline (salt water). This is a blinded study which means the participant will not know which group they have been assigned. The subjects participation will last 12 months (surveys post operatively).

Timeline

Start
2009-05
Primary completion
2011-10
Completion
2011-10

Outcome

Outcome not reported

Stopped: “PI terminated employment with the University”

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Lidocaine Other / unclassified 33.3 ug/kg Intravenous

Indications

No indication recorded.