Developing a Diabetic Foot Ulcer Protocol



Status:Completed
Conditions:Gastrointestinal, Podiatry, Diabetes
Therapuetic Areas:Endocrinology, Gastroenterology, Orthopedics / Podiatry
Healthy:No
Age Range:18 - Any
Updated:4/2/2016
Start Date:May 2010
End Date:December 2011
Contact:Talar L Glover, MS, RN, CNS
Email:talar_glover@hchd.tmc.edu
Phone:713-566-2513

Use our guide to learn which trials are right for you!

Developing a Diabetic Foot Ulcer Protocol in a Multi-ethnic, Underserved Population

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.

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.

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
We found this trial at
1
site
?
mi
from
Houston, TX
Click here to add this to my saved trials