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Completed

NCT Number: NCT04336176

Evaluating Plantar Foot Pressure in a Novel Diabetic Offloading Device

The impacts from diabetes are both patient related and healthcare based. Offloading is recognised as the priority treatment for healing neuropathic and neuro-ischaemic plantar foot ulcers. The new PulseFlow DF boot is a device which claims to off load but has little or no evidence on diabetic foot ulcer (DFU) subjects. Thus the primary aim of this study is to observe forefoot plantar pressures in a cross sectional purposively selected sample compared to usual standard of care.

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Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

The Leeds Teaching Hospitals NHS Trust.

Leeds, United Kingdom

About this study

The impacts from diabetes are both patient related and healthcare based. DFU is associated with a high mortality rate at 34% at 1 year. There is an associated higher limb amputation rate from DFU than other causes. The high mortality rate, high amputation rate and increased socio-economic burden means providing high quality evidence based DFU service provision should be a NHS priority. Offloading is recognised as the priority treatment for healing neuropathic and neuro-ischaemic plantar foot ulcers. Since the provision of non removable devices or total contact casts (TCC) is poor, options have to be available that are equivalent in effectiveness at off loading and healing DFU. By improving the quality of offloading choices and acceptability for devices this will improve healing rates and reduce the cost burden where currently in the UK diabetic foot care in 2015 accounted for 0.6%/585.5million pounds of the NHS budget. The evidence for effectiveness of non removable devices is poor. Therefore any device that offloads to the equivalent or more than previous devices and current usual standard of care must be evidenced. The new PulseFlow DF boot is such a device which claims to off load but has little or no evidence on DFU subjects. Thus the primary aim of this study is to observe forefoot plantar pressures in a cross sectional purposively selected sample compared to usual standard of care.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Plantar forefoot diabetic foot ulcer over the 1st, 2nd, 3rd, 4th or 5th MTP joints
  • Neuropathic or Neuro-Ischaemic classification foot ulcer (taken from the TEXAS classification system)
  • Orthotic intervention for offloading/usual standard
  • English speaking and reading
  • Palpable foot pulses and/or Ankle Brachial Pressure Indices of values 0.8 to 1.29.

Exclusion criteria

  • Being treated for or having an active Charcot Arthropathy
  • Ankle Brachial Pressure Indices of <0.8 and >1.29. Using a standardised reproducible instrument called the Huntleigh Dopplex Ability Unit (DA100PB).
  • Purely ischaemic classification foot ulcer
  • Clinically active Infection causing lower leg swelling
  • Current active osteomyelitis
  • Due to alterations in gait, patients with diagnosed vascular dementia, Parkinson's, alcoholism or other major medically related gait alterations i.e. intoxication, brain cancers, muscular degeneration diseases, inflammatory arthritis, etc. This does not include osteo-arthritis.
  • Fractures of the foot
  • Pregnancy
  • Patients with forefoot trans metatarsal or major amputations
  • Temporary, accommodating or footwear not designed to offload used as their USC
  • Under another trial regarding foot dressings or off loading -

Treatment and study plan

PulseFlow DF boot

Device

Offloading boot

Usual standard of care

Device

Usual standard of care (offloading device)

SHAM

Device

Sham shoe (closest to barefoot or baseline pressures)

Primary outcomes

  1. Pressure Time Integral

    Time frame: 1 day

    Gait analysis

Secondary outcomes

  1. Modified Monitoring Orthopaedic Shoes questionnaire

    Time frame: 1 day (post gait analaysis)

    Multiple choice questionnaire and visual analogue pain scale measuring relevant factors of use and usability of orthopaedic shoes from a patient's perspective.

Sponsors and collaborators

Lead sponsor

University of Leeds

Other

Collaborators

  • The Leeds Teaching Hospitals NHS Trust

Registry information

Official study title

Does a Novel Diabetic Foot Offloading Boot Reduce the Pressure Time Integral Compared to Usual Standard Care, in Patients With Diabetic Foot Ulcer? A Proof of Concept Pilot Study

Important dates

Study start
2018
Primary completion
2018
Study completion
2018
First posted
Apr 7, 2020
Registry last updated
Apr 7, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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