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Diabetes Peripheral Neuropathy and Small-fibre Nerve Damage: A Comparative Study

H

Haukeland University Hospital

Status

Completed

Conditions

Small Fibre Neuropathy
Autonomic Neuropathy
Peripheral Neuropathy
Diabetes Mellitus

Study type

Observational

Funder types

Other

Identifiers

NCT01160887
2010/1652

Details and patient eligibility

About

The purpose of this study is to investigate whether patients with diabetes-related peripheral neuropathic pain also have non-recognized damage to the intestine caused by autonomic neuropathy. The model will shed light on aspects of peripheral nerve injuries on both somatic and as well as visceral sensory nerves. Classical autonomic parameters from electrocardiography (ECG) and Holter (24-h ECG and blood pressure) are compared with peripheral nerve injuries. The damage of autonomic nerves often recognized late in the course when patients develop gastroparesis, however an earlier recognition of this nerve damage may help clarifying the fundamental pathomechanisms and thereby optimize treatment for this patient group in the future.

Enrollment

40 patients

Sex

All

Ages

18 to 75 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Male or female patients between 18 and 75 years with diagnosed diabetes mellitus, according to WHO criteria (World Health Organization).
  2. Proven peripheral neuropathy.
  3. Oral and written consent, with documentation that all relevant information about the program is given to the patient.
  4. The patient must be willing and able to, to meet the planned visit and meet the planned curriculum, including the participation in the experimental investigations.

Exclusion criteria

  1. Pregnancy or breastfeeding
  2. Medical or surgical disease for the study doctor's assessment makes the patient unsuitable for participation in the study
  3. Previous or ongoing major depression
  4. Patients who can or will not comply with the recommended instructions given by the study doctor
  5. Use of analgesic opioid medication less than 24 hours before screening
  6. Competitive conditions that can cause peripheral neuropathy (eg, herpes zooster)
  7. Clinically significant disease less than 2 weeks from the planned entry in the study
  8. People involved in the planning or execution of the study

Trial design

40 participants in 2 patient groups

Patients with diabetic peripheral neuropathy
Healthy matched controls

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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