Status:
COMPLETED
Safety and Efficacy of Gabapentin in Diabetic Peripheral Neuropathy
Lead Sponsor:
Depomed
Conditions:
Diabetic Peripheral Neuropathy
Eligibility:
All Genders
18+ years
Phase:
PHASE2
Brief Summary
The purpose of this study is to determine whether a new Gabapentin tablet, is safe and effective for the treatment of painful diabetic peripheral neuropathy.
Eligibility Criteria
Inclusion
- Men or women 18 years or older with diagnosis of type 1 or type 2 diabetes who have reported symmetrical painful symptoms in distal extremities for 1-5 years prior to the study and whose symptoms are attributable to sensorimotor diabetic peripheral neuropathy (DPN).
- Patients of childbearing potential must have a negative urine pregnancy test at screening/randomization, and must use medically acceptable methods of birth control.
- Patient has pain score of at least 4 on the 11-point Likert numerical rating scale at screening. Potential patients should not be informed of the pain intensity eligibility criterion prior to screening or randomization.
- Patient has a mean baseline week pain intensity of at least 4 on the 11-point Likert scale at the end of a one-week pre-treatment period and has completed at least 4 days of diary entries during the baseline week.
- Patient is on stable regimen of antidiabetes medication at screening that can be maintained during the study.
- Patient has hemoglobin A1c (HbA1c) ≤11% at screening.
- Patient has FPG ≤310 mg/dL at screening.
- Patient must have a minimum washout of greater than 5 times the half-life of the drug of any of several medications
- Patients currently treated with gabapentin or pregabalin at screening may be eligible for the study, but must have tapering period wherein the dose of gabapentin is reduced gradually over a period of at least 7 days plus a 2-day or 3-day washout of gabapentin or pregabalin, respectively, prior to start of the Baseline Week.
- Patient must have adequate eyesight to complete questions on the DiaryPro and SitePro. If a patient is unable to do so (for reasons other than severe eye disease) but a caregiver is available to complete these tasks following instruction from the patient, the caregiver may be trained to accomplish these tasks
Exclusion
- Patients who have previously not responded to treatment for DPN with gabapentin at doses of ≥1200 mg/day or pregabalin at doses ≥300 mg/day.
- Patients who previously experienced dose-limiting adverse effects that prevented titration of gabapentin to an effective dose.
- Patient has hypersensitivity to gabapentin.
- Patient is a nursing mother.
- Patient has used injected anesthetics or steroids within 30 days of baseline.
- Patient has certain conditions that could confound evaluation of painful DPN, in particular, amputations other than toes, non-diabetic neurologic disorders (e.g. phantom limb pain), and skin conditions affecting sensation in painful limbs.
- Patient has skin conditions in the area affected by the neuropathy that could alter sensation.
- Patient is in an immunocompromised state.
- Patient has an estimated creatinine clearance of \<60 ml/min calculated using the Cockroft Gault method (Appendix 3).
- Patient has had malignancy within past 2 years other than basal cell carcinoma.
- Patient has had gastric reduction surgery.
- Patient has severe chronic diarrhea, chronic constipation \[unless attributed to drugs that will be washed out\], uncontrolled irritable bowel syndrome (IBS) or unexplained weight loss.
- Patient has any abnormal chemistry or hematology results that are deemed by the investigator to be clinically significant.
- Patient has a history of substance abuse within the past year.
- Patient has had 1 or more visits to an emergency room or hospital within the previous 30 days due to hypoglycemia.
- Patient has a history of seizure (except for infantile febrile seizure) or is at risk of seizure due to head trauma.
- Patient has a history of pernicious anemia, untreated hypothyroidism, chronic hepatitis B or C, hepatitis within the past 3 months, or HIV infection.
- Patient has any other serious medical condition that, in the opinion of the Investigator would jeopardize the safety of the patient or affect the validity of the study results.
- Continuing use of any concomitant medication excluded by Inclusion Criterion 8.
- Patient has participated in a clinical trial of an investigational drug or device within 30 days of the screening visit
Key Trial Info
Start Date :
April 1 2006
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 1 2006
Estimated Enrollment :
147 Patients enrolled
Trial Details
Trial ID
NCT00712439
Start Date
April 1 2006
End Date
December 1 2006
Last Update
June 8 2011
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