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Clinical Trials/NCT01160887
NCT01160887
Completed
N/A

Is Diabetic Peripheral Neuropathy Accompanied by Internal Nerve Damage? A Comparative, Clinical Experimental Study of Peripheral and Visceral Nerve Damage in Diabetic Patients and Healthy Controls

Haukeland University Hospital1 site in 1 country40 target enrollmentJune 2010

Overview

Phase
N/A
Intervention
Not specified
Conditions
Diabetes Mellitus
Sponsor
Haukeland University Hospital
Enrollment
40
Locations
1
Primary Endpoint
glucose
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

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.

Registry
clinicaltrials.gov
Start Date
June 2010
End Date
July 2013
Last Updated
12 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Haukeland University Hospital
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Male or female patients between 18 and 75 years with diagnosed diabetes mellitus, according to WHO criteria (World Health Organization).
  • Proven peripheral neuropathy.
  • Oral and written consent, with documentation that all relevant information about the program is given to the patient.
  • 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

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

Outcomes

Primary Outcomes

glucose

Time Frame: one year

Study Sites (1)

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