Expired Study
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Pembroke Pines, Florida


Purpose:

The purpose of the study is to determine if duloxetine can help patients with painful diabetic neuropathy.


Study summary:

The protocol will assess the efficacy and safety of duloxetine. It will also look at how duloxetine affects quality of life.


Criteria:

Inclusion Criteria: - Male or female outpatients at least 18 years of age. - Patients with pain due to diabetic neuropathy in both legs. - Females must not be pregnant or plan to become pregnant during the study. - Stable Glycemic control. - Average mean pain severity score of at least 4.0 as assessed by completion of a daily diary. Exclusion Criteria: - You are related to or work for the physician conducting the study or are employed by Eli Lilly and Company. - You have a severe or serious medical condition that causes you to be hospitalized often; or you have had a kidney transplant or are on current dialysis. - You have participated in a study for an investigational drug within the last 30 days. - You have a history of major depressive disorder, generalized anxiety disorder, or alcohol or eating disorders. - You have a past medical history or diagnosis of mania, bipolar disorder, or psychosis.


NCT ID:

NCT00058968


Primary Contact:

Study Director
Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours EST)
Eli Lilly and Company


Backup Contact:

N/A


Location Contact:

Pembroke Pines, Florida
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: June 25, 2018

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