NCT Number: NCT00375960
A Research Study of V3381 for the Treatment of Diabetic Peripheral Neuropathic Pain
The objective of this study is to investigate the safety and efficacy of an investigational drug, V3381, for the treatment of diabetic peripheral neuropathic (DPN) pain (pain in one's feet and legs, or even in one's hands and arms, sometimes experienced by people with diabetes). An investigational drug is one that is not approved by the United States Food and Drug Administration (FDA) and/or Health Canada.
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Conditions
Age range
18 year–75 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 2
Primary location
LMC Endocrinology Centres Ltd., Thornhill, Ontario, Canada
About this study
Diabetic Peripheral Neuropathic Pain (DPNP) is pain in your feet and legs, or even in your hands and arms, sometimes experienced by people with diabetes. Neuropathic pain syndromes are much more common than is perhaps generally recognized. Approximately 1% of the population in western countries suffers from neuropathic pain. Some clinical conditions are associated with a relatively high incidence of neuropathic pain. Approximately 15% of patients with diabetic neuropathy have persistent neuropathic pain in the feet, legs and hands.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Males or females 18-75 years of age
- Diabetes mellitus (type I or type II)
- No change in medications for reducing blood sugar within 4 weeks before screening
- Experiencing daily pain due to diabetic neuropathy for at least 6 months but not more than 5 years
- Neuropathic pain must begin in the feet, with relatively symmetrical onset.
- Willing to perform self-monitoring of blood glucose
- Able to communicate intelligibly with the investigator and study coordinator
- Keeping all appointments for clinic visits, tests, and procedures
Exclusion criteria
- Any clinically significant neurologic disorders (with the exception of diabetic peripheral neuropathic pain)
- Any clinically significant or unstable medical or psychiatric condition that would interfere with the patient's ability to participate in the study
- Prior renal transplant or current renal dialysis
- Pernicious anemia
- Untreated hypothyroidism
- Amputations due to diabetes mellitus (with the exception of toes)
- Any clinically significant abnormal electrocardiogram (ECG)
- Any history of cardiac arrhythmia
- History of myocardial infarction
- Active angina
- Uncontrolled hypertension (i.e., > 140/90 mm Hg)
- Known or at high risk of hepatitis B or C infection
- Known or at high risk of human immunodeficiency virus (HIV) infection
- Any anticipated need for surgery during the study
- Glycosylated hemoglobin (HbA1c) > 9%
- Known seizure disorder
- Any malignancy in the past 2 years (with the exception of basal cell carcinoma)
- Pain that cannot be clearly differentiated from, or conditions that interfere with the assessment of diabetic neuropathic pain.
- Use of anticonvulsants, antidepressants, or prescription membrane-stabilizing agents
- History of substance abuse or dependence within the past year, excluding nicotine and caffeine
- Frequent and/or severe allergic reactions with multiple medications
- Participation in any clinical trial within 30 days before screening
Treatment and study plan
Placebo
DrugPrimary outcomes
-
11 point numerical pain rating scale (NPRS) daily diary
Secondary outcomes
-
Modified Brief Pain Inventory for DPN
-
McGill Pain Questionnaire - Short Form
-
Neuropathic Pain Symptom Inventory
-
Medical Outcomes Survey Short Form - 12, Version 2
-
Patient Global Impression of Change
-
Patient Preference Questionnaire (end of 2nd treatment period only)
-
Clinical Global Impression of Change
-
Additional secondary assessments will be included in the daily diary: consumption of rescue analgesics
-
daily sleep interference score
Sponsors and collaborators
Lead sponsor
Vernalis (R&D) Ltd
Industry
Collaborators
- Cita NeuroPharmaceuticals
Registry information
Official study title
A Randomized, Double-Blind, Placebo-Controlled, Multicenter, Crossover Study of the Safety, Efficacy and Pharmacokinetics of Two Escalating, Oral Doses of V3381 (200 mg BID and 400 mg BID) for 28 Days in Patients With Diabetic Peripheral Neuropathic Pain (DPNP)
Important dates
- Study start
- 2006
- Study completion
- 2007
- First posted
- Sep 13, 2006
- Registry last updated
- Apr 2, 2007
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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