The Effect of Pregabalin on Pain Related to Walking in Patients With Diabetic Peripheral Neuropathy

Eastern Virginia Medical School (EVMS)

Status and phase

Completed

Phase 3

Conditions

Nerve Pain

Diabetic Peripheral Neuropathy

Treatments

Drug: Pregabalin

Drug: Placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT02927951

10-11-FB-0209

Details and patient eligibility

About

The hypothesis of this study is that pregabalin, 150 mg bid, will reduce general daytime pain in patients diagnosed with diabetic peripheral neuropathy and that it will also reduce the level of pain associated with walking. Consequently, it is hypothesized that the reduction in pain will result in an increase in the amount of walking they do during the day, improvements in their gait, balance, risk of falls and sleep patterns.

Full description

Pregabalin (LYRICA®) is a potent and specific ligand at the alpha-2-delta subunit of voltage-gated calcium channels. It is currently approved for adjunctive therapy for neuropathic pain conditions. Patients with diabetic peripheral neuropathy suffer from pain in their feet which interferes with their ability to walk which includes less walking, an altered gait, and altered balance. At night the peripheral neuropathy also interferes with their sleep patterns.The hypothesis of this study is that pregabalin, 150 mg bid, will reduce general daytime pain in patients diagnosed with diabetic peripheral neuropathy and that it will also reduce the level of pain associated with walking. Consequently, it is hypothesized that the reduction in pain will result in an increase in the amount of walking they do during the day, improvements in their gait, balance, risk of falls and sleep patterns.Pain and sleep quality will be assessed with questionnaires but objective measurements will be used to assess gait, balance, daytime activities (including walking) and sleep patterns.

Statistical Power Calculations were based on the fact that this is a randomized, double-blind, placebo-controlled, 2-period crossover study to be conducted at a single site. Comparisons will be drawn at baseline, at the completion of each 6 weeks of treatment/placebo arm. The study has been powered at 0.80 for a two-tail analysis with a sensitivity to detect a 30% delta in pain perception in 40 subjects. From previous studies, the cross-over design suggested has achieved significance with 20 patients per group. Forty-four patients will be recruited in total. Significance will be established at an alpha level of 0.05. Both parametric and non parametric correlations will be carried out between the different variables measured and progressive logistic regression to determine the relative contributions of pain relief on the primary and secondary variables being measured in the study.

Enrollment

44 patients

Sex

All

Ages

40 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Individuals with painful, peripheral neuropathy (ages 40-75 years) and type 2 diabetes (n=40).

Exclusion criteria

Active ocular or systemic disease
Recent or recurrent history of musculoskeletal injury,
Presence of neurological conditions or idiopathic neuropathy
History of or vertigo
Use of an aid while walking or difficulty with standing upright
Visible tremor or uncorrected visual deficits.
Presence of type 1 diabetes mellitus (defined as C-peptide < 1 ng/ml or diabetes onset at < 35 years of age in a non-obese patient).
Presence of diabetic retinopathy that is more severe than "background" level.
Presence of diabetic nephropathy
Presence of clinically significant neuropathy that is clearly of non-diabetic origin, e.g. alcoholic or autoimmune.
Bilateral amputation of lower extremities or foot ulcers involving the great toes.
Presence of neuroarthropathy (Charcot deformity) is allowable.
History of major macrovascular events such as myocardial infarction or stroke within the past 6 months.
Patients with moderate or severe hepatic insufficiency or abnormalities of liver function.
Presence of significant pedal edema.
Other serious medical conditions that in the opinion of the investigator, would compromise the subject's participation in the study.