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Developing a Diabetic Foot Ulcer Protocol

Primary Purpose

Diabetic Foot Ulcers

Status
Withdrawn
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
type of footwear
collagen dressing with and without silver
Sponsored by
The University of Texas Health Science Center, Houston
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetic Foot Ulcers focused on measuring diabetes, foot ulcers, off-loading, collagen, Wagner 1

Eligibility Criteria

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

Inclusion Criteria:

  • Adult - over 18 years of age
  • Diabetes with an A1c of less than or equal to 9% - if no A1c result is available within the past 3 months, one will be drawn to qualify the patient for the study
  • No evidence of circulatory compromise

    • Posterior tibial or pedal pulse present on palpation
    • No pallor on elevation
    • No dependent rubor
  • Loss of sensation on forefoot using monofilament
  • Wound or callus on only 1 foot
  • Wound Classification - Wagner Grade 1, non-infected

    • Ulcer present for 1 - 3 months
    • Ulcer of forefoot only
    • No previous ulcer of that foot or amputation of either extremity
    • Wound size < 1" diameter
    • Wound bed pink

Exclusion Criteria:

  • Diagnoses with unpredictable trajectory or healing ability, i.e.

    • Psychiatric disorders
    • Cancer
    • ESRD not eligible for dialysis
    • HIV
  • Previous lower extremity amputation
  • Charcot foot
  • Evidence of circulatory compromise

    • Absence of pulses
    • Decreased capillary refill (> 3 seconds)
    • Trophic skin changes - shiny, hairless toes
    • Ankle Brachial Index < 0.8

Sites / Locations

  • Harris County Hospital District Community Health

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm 6

Arm Type

Active Comparator

Active Comparator

Active Comparator

Active Comparator

Active Comparator

Active Comparator

Arm Label

shoe, plain dressing

shoe, collagen

boot, plain dressing

boot, collagen

monitored air boot, plain dressing

monitored boot with collagen

Arm Description

post-op shoe with plain occlusive dressing

post-op shoe with collagen dressing

air boot with occlusive dressing

air boot with collagen dressing

air boot with retention strap to monitor whether boot is removed with occlusive dressing

air boot with retention strap to monitor whether boot is removed with collagen dressing

Outcomes

Primary Outcome Measures

decrease in size of wound

Secondary Outcome Measures

non-healing wound

Full Information

First Posted
February 11, 2010
Last Updated
November 3, 2020
Sponsor
The University of Texas Health Science Center, Houston
Collaborators
Harris County Hospital District, Baylor College of Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT01068171
Brief Title
Developing a Diabetic Foot Ulcer Protocol
Official Title
Developing a Diabetic Foot Ulcer Protocol in a Multi-ethnic, Underserved Population
Study Type
Interventional

2. Study Status

Record Verification Date
November 2020
Overall Recruitment Status
Withdrawn
Why Stopped
no patients who met enrollment criteria
Study Start Date
May 2010 (undefined)
Primary Completion Date
June 2012 (Anticipated)
Study Completion Date
June 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The University of Texas Health Science Center, Houston
Collaborators
Harris County Hospital District, Baylor College of Medicine

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to determine which treatment, over 6 months, will promote healing of diabetic foot ulcers that are not infected in the most efficient, cost-effective way.
Detailed Description
This pilot study will be conducted in Harris County Hospital District (HCHD) Community Health Centers and Wound Care Clinics. The study will use random assignment of patients who meet inclusion criteria to: postoperative shoe with or without collagen; removable Air-boot with or without collagen; or monitored Air-boot with or without collagen. All treatment is standard of care. Enrollment will occur at a clinic appointment. During the consent appointment, follow-up will be scheduled. Patients whose wound meets study criteria will be approached by a Podiatrist or therapist during a wound care visit. An A1c will be obtained, if not done within the past 3 months. A convenience sample will be drawn from people with diabetes, aged 18 or more, who meet inclusion criteria. Frequency of visits will be: patients with monitored Air-boot: weekly all others: every 2 weeks At each visit there will be a dressing change, wound assessment and review of how many times shoe/boot was removed or not used during the preceding 1 or 2 weeks. Should healing not occur within 6 months or the wound progress, the patient will be referred for evaluation of possible vascular involvement.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetic Foot Ulcers
Keywords
diabetes, foot ulcers, off-loading, collagen, Wagner 1

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
shoe, plain dressing
Arm Type
Active Comparator
Arm Description
post-op shoe with plain occlusive dressing
Arm Title
shoe, collagen
Arm Type
Active Comparator
Arm Description
post-op shoe with collagen dressing
Arm Title
boot, plain dressing
Arm Type
Active Comparator
Arm Description
air boot with occlusive dressing
Arm Title
boot, collagen
Arm Type
Active Comparator
Arm Description
air boot with collagen dressing
Arm Title
monitored air boot, plain dressing
Arm Type
Active Comparator
Arm Description
air boot with retention strap to monitor whether boot is removed with occlusive dressing
Arm Title
monitored boot with collagen
Arm Type
Active Comparator
Arm Description
air boot with retention strap to monitor whether boot is removed with collagen dressing
Intervention Type
Other
Intervention Name(s)
type of footwear
Other Intervention Name(s)
DJO XP Diabetic Walker, Camcon Medical postoperative shoe, Smith and Nephew Allevyn Foam dressing
Intervention Description
comparison of results between post-op shoe, air boot which the patient can remove ad lib and air boot whose removal can be monitored
Intervention Type
Other
Intervention Name(s)
collagen dressing with and without silver
Other Intervention Name(s)
Smith & Nephew Biostep dressing with Allevyn Foam cover, Smith & Nephew Biostep Ag gressing with Allevyn Foam cover
Intervention Description
silver-impregnated collagen dressing will be used for 2 weeks, then plain collagen dressing will be used for the remainder of the 6 months
Primary Outcome Measure Information:
Title
decrease in size of wound
Time Frame
6 months
Secondary Outcome Measure Information:
Title
non-healing wound
Time Frame
6 months or less

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult - over 18 years of age Diabetes with an A1c of less than or equal to 9% - if no A1c result is available within the past 3 months, one will be drawn to qualify the patient for the study No evidence of circulatory compromise Posterior tibial or pedal pulse present on palpation No pallor on elevation No dependent rubor Loss of sensation on forefoot using monofilament Wound or callus on only 1 foot Wound Classification - Wagner Grade 1, non-infected Ulcer present for 1 - 3 months Ulcer of forefoot only No previous ulcer of that foot or amputation of either extremity Wound size < 1" diameter Wound bed pink Exclusion Criteria: Diagnoses with unpredictable trajectory or healing ability, i.e. Psychiatric disorders Cancer ESRD not eligible for dialysis HIV Previous lower extremity amputation Charcot foot Evidence of circulatory compromise Absence of pulses Decreased capillary refill (> 3 seconds) Trophic skin changes - shiny, hairless toes Ankle Brachial Index < 0.8
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gary Lepow, DPM
Organizational Affiliation
University of Texas Health Science at Houston, Baylor College of Medicine
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Talar L Glover, MS, RN, CNS
Organizational Affiliation
Harris County Hospital District
Official's Role
Principal Investigator
Facility Information:
Facility Name
Harris County Hospital District Community Health
City
Houston
State/Province
Texas
ZIP/Postal Code
77054
Country
United States

12. IPD Sharing Statement

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Developing a Diabetic Foot Ulcer Protocol

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