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Electrical Stimulation in Diabetic Peripheral Neuropathy (NERVES)

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Imperial College London

Status

Completed

Conditions

NMES
Control

Treatments

Device: NMES

Study type

Interventional

Funder types

Other

Identifiers

NCT02082145
13HH1825 (Other Identifier)
13/LO/1844

Details and patient eligibility

About

To assess the effect of the device on the progression of diabetic peripheral neuropathy

Full description

Diabetes is a metabolic disease that affects the body's ability to control blood sugar levels. This affects the tissues of the body, particularly the walls of blood vessels. People with diabetes are more likely to suffer from ischaemic heart disease, stroke, kidney problems, blindness, foot ulcers, and peripheral nerve problems. Diabetes affects approximately 347 million people worldwide, and by 2030 the WHO projects that complications of diabetes will be the 7th leading cause of death.

Peripheral neuropathy is a dysfunction of the nerves most commonly affecting the arms and legs. Diabetes is the leading cause of neuropathy in the Western world, and diabetic neuropathy is estimated to affect between 20-50% of diabetic people. The American Diabetes Association define it as the 'presence of symptoms and signs of peripheral nerve dysfunction in patients with diabetes after exclusion of other causes'. As regards complications of diabetes, peripheral neuropathy has the greatest detrimental effect on quality of life. Diabetic neuropathy is implicated in 50-75% of non-traumatic amputations.

The device to be tested mimics the effect of walking by stimulating the motor nerves of the leg, making the foot twitch- it increases blood flow to the limb and exercises the leg muscles. We have seen previous clinical cases of improvement in peripheral neuropathy with use of the device, and wish to formalise the benefits to patients. It is hypothesised to work either by increasing blood flow to the limb and therefore the nerves themselves, or for electrical current to be having a direct effect on the peripheral nervous system itself. The device is easily fitted, can be self-administered by patients, and is suitable for out-patient therapy.

We wish to evaluate both the short- and longer-term effects of a neuromuscular stimulator on diabetic peripheral neuropathy as a therapeutic intervention.

Enrollment

14 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion criteria

  • 18+ years old
  • Diabetes as defined by WHO diagnostic criteria on best medical therapy
  • Diabetic peripheral polyneuropathy present, confirmed by nerve conduction testing

Exclusion criteria

  • Pregnancy
  • Pacemaker
  • Metal implants in the legs (below knee)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

14 participants in 2 patient groups

Control
No Intervention group
Description:
Treated according to local protocol for diabetic peripheral neuropathy
NMES
Experimental group
Description:
Treated with neuromuscular stimulation of both legs, for 10 weeks
Treatment:
Device: NMES

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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