Duloxetine vs. placebo in patients with painful diabetic neuropathy
Indiana University – Purdue University Indianapolis · Indiana University School of Medicine · +4 more institutions
Abstract
The aim of this study was to examine the efficacy and safety of duloxetine, a balanced and potent dual reuptake inhibitor of serotonin and norepinephrine, in the management of diabetic peripheral neuropathic pain. Serotonin and norepinephrine are thought to inhibit pain via descending pain pathways. In a 12-week, multicenter, double-blind study, 457 patients experiencing pain due to polyneuropathy caused by Type 1 or Type 2 diabetes mellitus were randomly assigned to treatment with duloxetine 20 mg/d (20 mg QD), 60 mg/d (60 mg QD), 120 mg/d (60 mg BID), or placebo. The diagnosis was confirmed by a score of at least 3 on the Michigan Neuropathy Screening Instrument. The primary efficacy measure was the weekly…
Citation impact
- FWCI
- 42.46
- Percentile
- 100%
- References
- 29
Authors
5- DGD. Goldstein
Indiana University – Purdue University Indianapolis, Indiana University School of Medicine
- YLYili Lu
Eli Lilly (United States)
- MJMichael J. DetkeCorresponding
McLean Hospital, Harvard University, Indiana University – Purdue University Indianapolis, Eli Lilly (United States), GTx (United States), Indiana University School of Medicine
- TCThomas C. Lee
Eli Lilly (United States)
- SISmriti Iyengar
Eli Lilly (United States)
Topics & keywords
- Duloxetine
- Medicine
- Placebo
- Duloxetine Hydrochloride
- Diabetic neuropathy
- Anesthesia
- Discontinuation
- Neuropathic pain
- Good health and well-being