Clinical Research study in patients with Diabetic Painful Neuropathy

Updated on 8 November 2020


Clinical Research study in patients with Diabetic Painful Neuropathy


Currently enrolling in your area! Is your current neuropathic pain treatment providing adequate control of your pain? If NOT, you may interested in learning more about a clinical research trial of an investigational medication that is being evaluated for the treatment of diabetes painful neuropathy. You may be eligible to participate if:

  • You are a male or female between the ages of 18 and 80
  • You have had persistent (chronic) pain for longer than six months due to diabetic painful neuropathy
If you qualify:
  • You will e reimbursed for study-related expenses
  • You will be provided clinical research-related medical care and study medication at no cost
We are actively seeking volunteers for this study.

Inclusion Criteria:

  • Chronic neuropathic pain (pain persistent for > 6 months) that is moderate to severe
  • Currently taking pain medication but are not adequately controlled by standard of care (which may include antidepressants, antiepileptics, topical lidocaine, or opioids), or are not currently taking pain medications because intolerable to, or not willing to use, standard of care

Exclusion Criteria:

  • Patients with severe diabetic neuropathy, defined by any 1 of the following: (1) Severe autonomic dysfunction and severe blood pressure instability, (2) Loss or decreased pinprick sensation above the knees or wrists (2) Women who are pregnant or breast-feeding

Clinical Study IdentifierTX134968
Last Modified on8 November 2020


How to participate?

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What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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