Full Text View
Tabular View
No Study Results Posted
Related Studies
Three Way Interaction Between Gabapentin, Duloxetine, and Donepezil in Patients With Diabetic Neuropathy
This study is currently recruiting participants.
Study NCT00619983   Information provided by Wake Forest University
First Received: February 8, 2008   Last Updated: August 14, 2009   History of Changes

February 8, 2008
August 14, 2009
February 2008
April 2010   (final data collection date for primary outcome measure)
Pain intensity measurements will be recorded twice daily, using McGill short form pain questionnaire on the PDA. The Visual Analog Pain Scale (VAS) will serve as the primary outcome measure. [ Time Frame: Study completion (16 weeks) ] [ Designated as safety issue: No ]
Pain intensity measurements will be recorded twice daily, using McGill short form pain questionnaire on the PDA. The Visual Analog Pain Scale (VAS) will serve as the primary outcome measure. [ Time Frame: Study completion ] [ Designated as safety issue: No ]
Complete list of historical versions of study NCT00619983 on ClinicalTrials.gov Archive Site
 
 
 
Three Way Interaction Between Gabapentin, Duloxetine, and Donepezil in Patients With Diabetic Neuropathy
Three Way Interaction Between Gabapentin, Duloxetine, and Donepezil in Patients With Diabetic Neuropathy

The purpose of the study is to determine whether the combination of the the three drugs gabapentin, duloxetine, and donepezil are effective in treating pain in people with diabetic neuropathy or patients with failed low back syndrome (chronic back pain).

Neuropathic pain is a complex and likely heterogeneous disorder, and we recognize that clinically useful agents such as opioids, gabapentin, and antidepressants may be effective precisely because they have multiple mechanisms of action at multiple sites. This study, however, will not only provide important mechanistic information regarding one cascade which can be manipulated for analgesia, but will also provide much needed systematic and practical guidance for multi-drug therapy in patients with neuropathic pain.

This study in patients with diabetic neuropathic pain and patients with failed low back syndrome, culminate in a quantitative description of interactions between activators of descending noradrenergic activity, norepinephrine transporter inhibitors, and cholinesterase inhibitors to exploit the plasticity of analgesia in chronic pain states. We will focus on practical applications, using clinically approved drugs, including gabapentin (Neurontin®) to activate noradrenergic activity, duloxetine (Cymbalta®) to inhibit the norepinephrine transporter, and donepezil (Aricept®), approved for the treatment of Alzheimer's dementia, but not previously tested to treat neuropathic pain, to inhibit cholinesterase.

After the baseline measurements and physical examination patients will be trained to use a Personal Digital Assistant (PDA) to answer questions about their diabetic neuropathic pain or their chronic back pain. Upon successful completion of these tasks the patients will be randomized to receive one of the drug choices or placebo (inactive pill).

The study will last for a total of 16 weeks and includes 5 visits to the research center with each visit lasting approximately 2 hours.

 
Interventional
Treatment, Randomized, Double Blind (Subject, Investigator, Outcomes Assessor), Parallel Assignment
  • Diabetic Neuropathic Pain
  • Chronic Low Back Pain
  • Drug: donepezil
  • Drug: duloxetine
  • Drug: donepezil 2.5 mg and duloxetine 30mg
  • Drug: placebo
  • Drug: gabapentin
  • Active Comparator: Donepezil 5 mg once per day for 12 weeks. Gabapentin will be added to all groups at week 9.
  • Active Comparator: Group 2: Will receive duloxetine 30 mg twice a day for 12 weeks. Gabapentin will be added to all groups at week 9.
  • Active Comparator: Group 3: Will receive a combination of donepezil 2.5 mg and duloxetine 30mg for 12 weeks. Gabapentin will be added to all groups at week 9.
  • Placebo Comparator: Group 4:Will receive placebo pills. Gabapentin will be added to all groups at week 9.
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Recruiting
60
July 2010
April 2010   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Diagnosis of diabetic neuropathy
  • Age 18-80
  • Willing to temporarily discontinue gabapentin or monoamine reuptake inhibitors upon entry into the study

Exclusion Criteria:

  • Pregnancy
  • Allergy to study medications
  • Uncontrolled narrow-angle glaucoma
  • Currently being treatment with thioridazine (Mellaril)
  • Unstable medical conditions including cardiac, pulmonary, renal or hepatic diseases
  • Treatment with a monoamine oxidase inhibitor (MAOI) within 14 days of randomization
Both
18 Years to 80 Years
No
Contact: Regina Curry, RN, CCRC 336-716-4294 recurry@wfubmc.edu
United States
 
NCT00619983
James C. Eisenach, M.D., Wake Forest University Health Sciences
IRB00003943, NS59574
Wake Forest University
National Institute of Neurological Disorders and Stroke (NINDS)
Principal Investigator: James C Eisenach, MD Wake Forest University
Wake Forest University
August 2009

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP