Surface NeuroMuscular Electrical Stimulation in the Treatment of Chronic Venous Leg Ulcers
NCT ID: NCT01801891
Last Updated: 2014-12-12
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE2
25 participants
INTERVENTIONAL
2013-05-31
2014-10-31
Brief Summary
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Detailed Description
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Surface neuromuscular electrical stimulation (SNMES) is the application of an electrical stimulus to motor points in the body using electrodes placed on the surface of the skin to elicit a muscular contraction. It has been shown that SNMES of the calf muscles, when used in conjunction with compression therapy, provides improved venous flow velocities over compression therapy alone. Furthermore, the week-long effect of SNMES and compression therapy on healthy participants was found to be well tolerated by all participants and resulted in increases in stimulated venous flow and muscle strength. A combined SNMES and compression treatment protocol which stimulates peripheral venous blood flow may help to alleviate harmful venous pressures in venous leg ulcer patients and provide some degree of strengthening of the calf muscles, thus helping to accelerate the healing rates of venous ulcers.
Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
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Control group
Patients randomised to the control group will, in addition to their routine compression bandaging, be given muscle stimulators for home use and instructed to apply 3x 30 minute sessions of comfortable electrical stimulation daily for 12 weeks. The stimulators given to the control group will be set to provide minimal stimulation resulting in no visible muscular contraction.
Compression bandaging
Compression bandaging systems apply graduated external pressure to the lower limb to promote venous return to the heart reducing venous hypertension and thereby facilitate venous ulcer healing.
VASGARD stimulator
Patients randomised to this group, in addition to their routine treatment with compression bandaging, will be given muscle stimulators for home use and instructed to apply 3x 30 minute sessions of comfortable electrical stimulation daily for 12 weeks. The intervention group stimulators will be capable of causing muscular contraction with a maximum force ranging from 30-40% of voluntary contractions.
VASGARD stimulator
The VASGARD device is a 2 channel muscle stimulator system designed for increasing venous blood flow. Controlled electrical stimuli are delivered to the patient through adhesive gel electrodes placed over the motor points of muscles on the lower leg. This elicits artificial muscular contractions which in turn increases lower limb venous haemodynamics.
Compression bandaging
Compression bandaging systems apply graduated external pressure to the lower limb to promote venous return to the heart reducing venous hypertension and thereby facilitate venous ulcer healing.
Interventions
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VASGARD stimulator
The VASGARD device is a 2 channel muscle stimulator system designed for increasing venous blood flow. Controlled electrical stimuli are delivered to the patient through adhesive gel electrodes placed over the motor points of muscles on the lower leg. This elicits artificial muscular contractions which in turn increases lower limb venous haemodynamics.
Compression bandaging
Compression bandaging systems apply graduated external pressure to the lower limb to promote venous return to the heart reducing venous hypertension and thereby facilitate venous ulcer healing.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Ankle-brachial pressure index \> 0.8
* Ulcer size between 1 and 200 cm2
* Patient suitable for full compression bandaging
Exclusion Criteria
* Pregnancy
* Presence of implants in the lower leg or a pacemaker
* History of a neurological disorder
* Presence of any contraindications for the use of compression stockings such as severe arterial disease i.e. Ankle brachial pressure index (ABPI) \<0.8
* Presence of cognitive difficulties which may prevent the patient or his/her carer from using the stimulator appropriately.
* Patients unable to provide informed consent
* Patients receiving dialysis
* Patients receiving steroids
* Patients receiving methotrexate
* Ulcer located in the area of electrode placement
* Patients in reduced compression bandaging system
18 Years
ALL
No
Sponsors
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Professor Stewart Walsh
OTHER
Responsible Party
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Professor Stewart Walsh
Professor Stewart Walsh
Principal Investigators
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Pierce A Grace, MCh FRCSI
Role: PRINCIPAL_INVESTIGATOR
HSE
Locations
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Department of Electronic Engineering, National University Ireland Galway
Galway, , Ireland
MidWestern Regional Hospital
Limerick, , Ireland
Countries
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Other Identifiers
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VASGARD2013
Identifier Type: -
Identifier Source: org_study_id