View Clinical Trial (Medical Research Study)
Double Blind RCT of Bicifadine SR in Outpatients With Chronic Neuropathic Pain Associated With Diabetes - NCT00553592-42003(Clinical Trial 189709)
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| City: |
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Paducah |
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State:
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KY |
| Zip Code: |
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42003 |
| Conditions: |
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Diabetic Peripheral Neuropathy |
| Purpose: |
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To compare the efficacy of two dosages (600mg/day and 1200mg/day) of bicifadine SR with
placebo for 14 weeks in reduction of chronic neuropathic patin (measured by a daily rating
of pain intensity) associated with diabetic periperal neuropathy in adult outpatients.
To compare the tolerability of two dosages of bicifadine SR with placebo in adult outpaitens
treated for chronic neuropathic pain for 14 weeks associated with diabetic peripheral
neuropathy.
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| Study summary: |
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| Criteria: |
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Inclusion Criteria:
- Male or female, 18 years or older
- Diagnosis of type-1 or type 2 non-insulin dependent diabetes mellitus
- Chronic bilateral pain due to diabetic neuropathy
- Pain for at least six months
- Primary pain is located in the feet
- Others-contact site for information
Exclusion Criteria:
- Symptoms of other painful conditions
- Presence of amputations other than toes
- Clinically significant psychiatric or other neurological disorder
- Use of certain medications
- Clinically important other diseases
- Pregnancy
- History of alcohol or narcotic abuse within two years
- Others-contact site for information |
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| Study is available at: |
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Four Rivers Clinical Research
Paducah, KY 42003
United States
Primary Contact:
Jesse Wallace, MD
Email: diargent@fourriversresearch.com
Phone: 270-441-4606
Secondary Contact:
Ivy Raso
Email: iraso@xtlbio.com
Phone: 845-267-0707 |
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If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
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| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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March 22, 2011 |
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