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Extracorporeal Shockwave Therapy for Diabetic Foot Wounds

Primary Purpose

Diabetic Foot, Wound

Status
Unknown status
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Extracorporeal shockwave therapy
Standard Wound Care
Sponsored by
Hull University Teaching Hospitals NHS Trust
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetic Foot focused on measuring Diabetic Foot Wound

Eligibility Criteria

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

Inclusion Criteria:

  • Diagnosis of diabetes mellitus
  • Open surgical wound of the foot
  • ABPI >0.8
  • Age greater than 18 years old
  • Able and willing to give written informed consent
  • Be able to adhere to protocol and attend all follow up appointments

Exclusion Criteria:

  • Pregnancy or breast-feeding
  • Current malignancy
  • Allergy to materials used in the treatment
  • Palliative
  • Unable or unwilling to give consent
  • Anticoagulation

Sites / Locations

  • Hull and East Yorkshire Hospitals NHS Trust

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Extracorporeal shockwave therapy

Standard wound care

Arm Description

The shockwave therapy will be given at 120 pulses/cm2, penetration 5mm at a dose of 0.1mJ/mm2 at 5 pulses/second (17). Participants will receive 3 sessions of shockwave therapy in a 7-day period. In addition to standard wound care (dressing changes, negative pressure wound therapy, debridement, offloading footwear, glycaemic control and antibiotics, where appropriate).

Patient with a diabetic foot wound who receive standard wound care, consisting of dressing changes, negative pressure wound therapy, debridement, offloading footwear, glycaemic control and antibiotics, where appropriate.

Outcomes

Primary Outcome Measures

Wound volume
Change in wound volume between study visits

Secondary Outcome Measures

Pain Score Questionnaire
Brief Pain Inventory and Visual Analogue Scale
Quality of Life Questionnaire
SF-12 and EQ-5Q-3L
Infection rate
The number of wounds which develop an infection in the study period
Amputation rate
The number of amputations of treated sites in the study period
Local perfusion rate
blood flow perfusion rate of superficial tissues using Doppler flowmetry
Tissue integrity
Tissue hydration determined by a vapometer

Full Information

First Posted
July 11, 2019
Last Updated
December 21, 2021
Sponsor
Hull University Teaching Hospitals NHS Trust
Collaborators
University of Hull
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1. Study Identification

Unique Protocol Identification Number
NCT04042285
Brief Title
Extracorporeal Shockwave Therapy for Diabetic Foot Wounds
Official Title
Extracorporeal Shockwave Therapy for Diabetic Foot Wounds: A Cohort Study Comparing Extracorporeal Shockwave Therapy to Standard Treatment for Diabetic Foot Wounds
Study Type
Interventional

2. Study Status

Record Verification Date
October 2021
Overall Recruitment Status
Unknown status
Study Start Date
February 1, 2019 (Actual)
Primary Completion Date
December 3, 2019 (Actual)
Study Completion Date
May 20, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hull University Teaching Hospitals NHS Trust
Collaborators
University of Hull

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
Diabetic wounds post digital amputation have poor healing in 30-45% of cases, resulting in 75% of patients undergoing a further amputation within the year, despite best wound management. Extracorporeal shockwave therapy is a promising safe and non invasive treatment that has been shown to improve healing in chronic ulcers and burns by promoting healing and decreasing risk of infection. The study will recruit patients on a hospital ward who have undergone a toe amputation for a infected non healing diabetic foot ulcer. Participants will be informed about the study, given an patient information sheet and invited to give informed consent. Consenting participants will undergo shockwave therapy three times in the seven days after their operation, in addition to standard wound care. Wound measurements, blood perfusion, tissue integrity, quality of life and pain scores will be recorded at baseline, after the third treatment, 4 weeks, 8 weeks and 12 weeks after recruitment to the study. The study aims to recruit 25 patients. The results will be compared to a matched retrospective cohort group who received standard wound care.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
25 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Extracorporeal shockwave therapy
Arm Type
Active Comparator
Arm Description
The shockwave therapy will be given at 120 pulses/cm2, penetration 5mm at a dose of 0.1mJ/mm2 at 5 pulses/second (17). Participants will receive 3 sessions of shockwave therapy in a 7-day period. In addition to standard wound care (dressing changes, negative pressure wound therapy, debridement, offloading footwear, glycaemic control and antibiotics, where appropriate).
Arm Title
Standard wound care
Arm Type
Placebo Comparator
Arm Description
Patient with a diabetic foot wound who receive standard wound care, consisting of dressing changes, negative pressure wound therapy, debridement, offloading footwear, glycaemic control and antibiotics, where appropriate.
Intervention Type
Device
Intervention Name(s)
Extracorporeal shockwave therapy
Intervention Description
Extracorporeal shockwave therapy will be given at 120 pulses/cm2, penetration 5mm at a dose of 0.1mJ/mm2 at 5 pulses/second. Participants will receive 3 sessions of shockwave therapy in a 7-day period.
Intervention Type
Other
Intervention Name(s)
Standard Wound Care
Intervention Description
dressing changes, negative pressure wound therapy, offloading footwear, debridement, glycaemic control and antibiotics as necessary
Primary Outcome Measure Information:
Title
Wound volume
Description
Change in wound volume between study visits
Time Frame
Baseline, up to 7 days, 4 weeks, 8 weeks, 12 weeks
Secondary Outcome Measure Information:
Title
Pain Score Questionnaire
Description
Brief Pain Inventory and Visual Analogue Scale
Time Frame
Baseline, 4 weeks, 8 weeks, 12 weeks
Title
Quality of Life Questionnaire
Description
SF-12 and EQ-5Q-3L
Time Frame
Baseline, 4 weeks, 8 weeks, 12 weeks
Title
Infection rate
Description
The number of wounds which develop an infection in the study period
Time Frame
Recorded at evey study contact
Title
Amputation rate
Description
The number of amputations of treated sites in the study period
Time Frame
Recorded at every study contact
Title
Local perfusion rate
Description
blood flow perfusion rate of superficial tissues using Doppler flowmetry
Time Frame
Baseline, up to 7 days
Title
Tissue integrity
Description
Tissue hydration determined by a vapometer
Time Frame
Baseline, up to 7 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of diabetes mellitus Open surgical wound of the foot ABPI >0.8 Age greater than 18 years old Able and willing to give written informed consent Be able to adhere to protocol and attend all follow up appointments Exclusion Criteria: Pregnancy or breast-feeding Current malignancy Allergy to materials used in the treatment Palliative Unable or unwilling to give consent Anticoagulation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
George E Smith, M.D
Organizational Affiliation
Academic Vascular Surgery Unit
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hull and East Yorkshire Hospitals NHS Trust
City
Hull
ZIP/Postal Code
HU3 2JZ
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
No

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Extracorporeal Shockwave Therapy for Diabetic Foot Wounds

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