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Diabetic Neuropathies clinical trials

View clinical trials related to Diabetic Neuropathies.

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NCT ID: NCT00861042 Completed - Clinical trials for Painful Diabetic Neuropathy

An Open-label follow-on Trial to Assess the Long-term Safety and Efficacy of Oral SPM 927 in Subjects With Diabetic Neuropathy

Start date: April 2002
Phase: Phase 2
Study type: Interventional

The primary objective of the trial is to assess the tolerability and safety of long-term SPM 927 administration in subjects with diabetic neuropathy.

NCT ID: NCT00858351 Completed - Clinical trials for Diabetic Neuropathy, Painful

Thermal Biofeedback for the Treatment of Diabetic Neuropathy

Start date: November 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to examine potential treatment options for a condition in diabetics that causes tingling, pain, and numbness in the hands and /or feet, also known as diabetic peripheral neuropathy.

NCT ID: NCT00857623 Completed - Pain Clinical Trials

Study to Evaluate the Analgesic Efficacy of 28 Days' Oral Administration of AZD2066 Compared With Placebo in Patients With Painful Diabetic Neuropathy

Start date: February 2009
Phase: Phase 2
Study type: Interventional

The purpose of this study is to investigate if AZD2066 can relieve the pain arising from painful diabetic neuropathy compared to placebo.

NCT ID: NCT00855439 Completed - Clinical trials for Type 2 Diabetes Mellitus

Evaluation of Exenatide in Patients With Diabetic Neuropathy

Start date: June 2008
Phase: N/A
Study type: Interventional

This study will look at whether or not the medication exenatide improves signs and symptoms of diabetic peripheral neuropathy in people with type 2 diabetes and mild to moderate diabetic peripheral neuropathy.

NCT ID: NCT00844194 Completed - Clinical trials for Depressive Disorder, Major

Duloxetine in Patients With Diabetic in Peripheral Neuropathic Pain With or Without Co-morbid Major Depressive Disorder

Start date: February 2009
Phase: Phase 4
Study type: Interventional

The primary objective is to evaluate, separately in diabetic polyneuropathic pain (DPNP) patients with and without co-morbid major depressive disorder (MDD), whether duloxetine given as 60 mg to 120 mg once daily (QD) leads to a clinically relevant improvement as measured by the change in Brief Pain Inventory (BPI) 24 hours average interference score from baseline to after 12 weeks. A clinically relevant improvement will be demonstrated if the confidence interval for the mean change from baseline does not lie above the clinically relevant change of -1.35. If statistically significant results are obtained for the DPNP patients with MDD, then the same evaluation will be performed for the DPNP patients without MDD in another confirmatory analysis. As secondary objectives the study will compare the two groups (MDD+/MDD-) regarding efficacy of duloxetine on BPI severity scales, the distribution of different percentages of pain reduction among the patient population, and the patients and physicians impressions of severity and improvement of pain. The study will also compare treatment outcomes regarding patient-relevant functionality and quality of life (QoL) between the two groups (MDD+/MDD-) by evaluating each single BPI interference item, the Short Form 12 (SF-12) Health Questionnaire and the West Haven Multidimensional Pain Inventory (MPI). As a third group of secondary objectives the efficacy of duloxetine of the psychological symptoms (e.g. depression) of DPNP patients with or without depression will be assessed using the Hamilton depression scale, the Beck Depression Inventory-II and the hospital Anxiety and Depression Scale. Further the effect of duloxetine treatment on fasting blood glucose (FBG) and hemoglobin A1c (HbA1c) will be evaluated. To monitor safety and tolerability, treatment discontinuation rates, treatment emergent adverse events, change in vital signs, laboratory results and suicidal thoughts will be assessed.

NCT ID: NCT00838799 Completed - Clinical trials for Diabetic Peripheral Neuropathic Pain

Study of the Safety and Efficacy of RGH-896 in Patients With Diabetic Peripheral Neuropathic Pain

Start date: February 2009
Phase: Phase 2
Study type: Interventional

This study is designed to evaluate the safety and efficacy of RGH-896 in patients with diabetic peripheral neuropathic pain.

NCT ID: NCT00837941 Withdrawn - Clinical trials for Painful Diabetic Neuropathy

A Study of Single Dose Pain Therapy in Patients With Painful Diabetic Neuropathy (0000-115)

Start date: April 2009
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine if analgesic efficacy can be detected with single dose administration in patients with chronic neuropathic pain due to painful diabetic neuropathy.

NCT ID: NCT00835757 Completed - Clinical trials for Diabetic Peripheral Neuropathy

Diffusion Tensor Imaging of Sural Nerves in Diabetic Peripheral Neuropathy

Start date: September 2008
Phase: N/A
Study type: Observational

This study aims to validate magnetic resonance imaging and diffusion tensor imaging (MRI/ DTI) analysis as a non-invasive method for the assessment of myelinated nerve fibers loss in diabetic peripheral neuropathy.

NCT ID: NCT00830011 Completed - Diabetic Neuropathy Clinical Trials

Cognitive Behavioral Therapy for Painful Diabetic Neuropathy

Start date: September 2004
Phase: N/A
Study type: Interventional

The primary objective of this study is to evaluate the usefulness of cognitive behavioral therapy (CBT) for the management of painful diabetic neuropathy. Participants will be randomly assigned to one of two treatment conditions: CBT plus standard medical care or standard medical care alone. CBT will be offered in ten, ninety-minute group sessions and will be provided by a psychologist with experience in the management of both diabetes and chronic pain. CBT will involve teaching and encouraging practice of adaptive pain coping skills such as relaxation skills, activity pacing, and positive self-statements, among others. This study will allow us to determine which treatment is superior in terms of improvements in pain management, functioning and overall quality of life.

NCT ID: NCT00829387 Completed - Clinical trials for Diabetic Peripheral Neuropathic Pain

Cognitive Behavioral Therapy for Diabetic Neuropathic Pain

Start date: March 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the efficacy of a brief psychological intervention, cognitive-behavior therapy, for the management of persistent pain associated with diabetic peripheral neuropathic pain.