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Evaluating Plantar Foot Pressure in a Novel Diabetic Offloading Device

Primary Purpose

Diabetic Foot Ulcer

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
PulseFlow DF boot
Usual standard of care
Sham
Sponsored by
University of Leeds
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional device feasibility trial for Diabetic Foot Ulcer

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

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

Exclusion Criteria:

  1. Being treated for or having an active Charcot Arthropathy
  2. Ankle Brachial Pressure Indices of <0.8 and >1.29. Using a standardised reproducible instrument called the Huntleigh Dopplex Ability Unit (DA100PB).
  3. Purely ischaemic classification foot ulcer
  4. Clinically active Infection causing lower leg swelling
  5. Current active osteomyelitis
  6. 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.
  7. Fractures of the foot
  8. Pregnancy
  9. Patients with forefoot trans metatarsal or major amputations
  10. Temporary, accommodating or footwear not designed to offload used as their USC
  11. Under another trial regarding foot dressings or off loading -

Sites / Locations

  • The Leeds Teaching Hospitals NHS Trust.

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Sham Comparator

Arm Label

PulseFlow DF boot

Usual Care

Sham

Arm Description

PulseFlow DF boot

Measurements will be taken from patients wearing usual standard of care

Sham shoe (closest to barefoot or baseline pressures)

Outcomes

Primary Outcome Measures

Pressure Time Integral
Gait analysis

Secondary Outcome Measures

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

Full Information

First Posted
March 26, 2020
Last Updated
April 6, 2020
Sponsor
University of Leeds
Collaborators
The Leeds Teaching Hospitals NHS Trust
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1. Study Identification

Unique Protocol Identification Number
NCT04336176
Brief Title
Evaluating Plantar Foot Pressure in a Novel Diabetic Offloading Device
Official 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
Study Type
Interventional

2. Study Status

Record Verification Date
April 2020
Overall Recruitment Status
Completed
Study Start Date
March 22, 2018 (Actual)
Primary Completion Date
June 29, 2018 (Actual)
Study Completion Date
July 29, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Leeds
Collaborators
The Leeds Teaching Hospitals NHS Trust

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
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.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetic Foot Ulcer

7. Study Design

Primary Purpose
Device Feasibility
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Proof of concept study comparing the ability to redistribute forefoot pressure using a new foot offloading device compared to usual standard care. The sample will be purposively selected taken from a local population of active diabetic foot ulcer patients. The measurements will be taken from patients wearing usual standard of care, sham shoe (closest to barefoot or baseline pressures) and the PulseFlow DF boot. The measurements from each patient will be collated to compute pti averages for the comparison
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
12 (Actual)

8. Arms, Groups, and Interventions

Arm Title
PulseFlow DF boot
Arm Type
Active Comparator
Arm Description
PulseFlow DF boot
Arm Title
Usual Care
Arm Type
Active Comparator
Arm Description
Measurements will be taken from patients wearing usual standard of care
Arm Title
Sham
Arm Type
Sham Comparator
Arm Description
Sham shoe (closest to barefoot or baseline pressures)
Intervention Type
Device
Intervention Name(s)
PulseFlow DF boot
Intervention Description
Offloading boot
Intervention Type
Device
Intervention Name(s)
Usual standard of care
Intervention Description
Usual standard of care (offloading device)
Intervention Type
Device
Intervention Name(s)
Sham
Intervention Description
Sham shoe (closest to barefoot or baseline pressures)
Primary Outcome Measure Information:
Title
Pressure Time Integral
Description
Gait analysis
Time Frame
1 day
Secondary Outcome Measure Information:
Title
Modified Monitoring Orthopaedic Shoes questionnaire
Description
Multiple choice questionnaire and visual analogue pain scale measuring relevant factors of use and usability of orthopaedic shoes from a patient's perspective.
Time Frame
1 day (post gait analaysis)

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
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 -
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anne-Maree Keenan, PhD
Organizational Affiliation
University of Leeds
Official's Role
Study Chair
Facility Information:
Facility Name
The Leeds Teaching Hospitals NHS Trust.
City
Leeds
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
No

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Evaluating Plantar Foot Pressure in a Novel Diabetic Offloading Device

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