Diabetic Foot Ulcer
Conditions
Keywords
diabetic peripheral neuropathy, diabetic foot, placenta stem cells
Brief summary
The purpose of this research study is to test the safety of placental stem cells to treat non-healing diabetic foot ulcers.
Detailed description
This is a prospective, non-randomized, single institution, Phase 1 safety trial to evaluate the safety of placental stem cells and the rate of diabetic foot ulcer healing in a population of subjects with non-healing diabetic foot ulcers for at least 4 weeks. The trial will also explore the clinical outcomes of placental stem cells treatment on diabetic peripheral neuropathy. Furthermore, the trial will evaluate the effect of the placental stem cells on serum biomarkers associated with diabetic foot ulcers and diabetic peripheral neuropathy (measured pre- and post-treatment) and correlate the biomarker levels with any changes in diabetic foot ulcers and diabetic peripheral neuropathy. Twelve adult subjects with non-healing diabetic foot ulcers for at least four weeks from diagnosis and not more than 12 months with wound sizes ≥ 2 cm2 and ≤ 4 cm2 will be recruited and treated. Subjects will be followed for 12 months after treatment.
Interventions
DRUGPlacenta Stem Cells
Injection of 30 M placenta stem cells into/around the diabetic foot ulcer and along the anterior and posterior tibial arteries of the index leg.
Sponsors
Wake Forest University Health Sciences
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Diagnosed with Type 2 Diabetes mellitus (DM) - for at least 1 year * Unilateral non-healing Diabetic Foot Ulcer (DFU) \> 2 cm2 and ≤ 4 cm2 (length × width) for at least four weeks despite Atrium Health Wake Forest Baptist standard of care treatment (which can include total contact cast, knee high air cast, and/or compression wrap) * No new diabetes medication for at least 2 weeks pre-treatment * Subjects must be willing to avoid steroids for the week prior to procedure day
Exclusion criteria
* Clinical signs of active infection requiring systemic antibiotic therapy less than 7 days prior to enrollment. * Radiographic or clinical evidence of active and untreated osteomyelitis at the target ulcer site. Current use of systemic immunosuppressive therapy, including chronic corticosteroids (equivalent to \>10 mg/day prednisone for \>14 days). * Hemoglobin (Hgb) A1C \>12.0 at screening or time in range for the blood glucose level (TIR) less than 30%. Hb A1c should not be used for patient with hypoalbuminemia or anemia in the past 3 months and for patients with Chronic Kidney disease stage 4. For patients who have Continuous Glucose Monitor (CGM), instead of Hb A1c, TIR (time in range) less than 30 % will be used. * Patients who are unable / unwilling to tolerate an effective offloading approach. This includes total contact cast, soft felted cast or knee high fracture boot. * Current alcohol or substance abuse that, in the opinion of the investigators, would interfere with study participation. * Active malignancy or malignancy related limb amputation. * Women that are pregnant or planning to become pregnant during the study. * Patients with albumin levels less than 3.5 or prealbumin levels less than 18. * Subjects with any conditions that the clinical Investigator believes may jeopardize the safety of the patient to participate in the trial. * Severe peripheral arterial disease (PAD) (Ankle-Brachial Index (ABI) less than 0.5) or TCOM (Transcutaneous Oximetry Measurement) less than 40 mmHg. * TWSB \> 30 cm2 (total wound surface burden)
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Number of Injection Sites Bleeding | Month 1 | Number of Injection Sites Bleeding |
| Number of Injection Sites infection/inflammation | Month 1 | Number of Injection Sites infection/inflammation |
| Number of Injection Sites with damage to surrounding tissue | Month 1 | Number of Injection Sites with damage to surrounding tissue |
| Number of Subjects with pain | Month 1 | Number of Subjects with pain |
| Number of Subjects with allergic reaction to placental cells | Month 1 | Number of Subjects with allergic reaction to placental cells |
| Number of Subjects with worsening of wound | Month 1 | Number of Subjects with worsening of wound |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Diabetic Foot Ulcer (DFU) size | Month 12 | DFU healing in this trial will be assessed by measuring the size of the DFU and plotting open wound size over the 12-month follow-up period. |
Countries
United States
Contacts
CONTACTMary-Clare Day, RN
PRINCIPAL_INVESTIGATORLucian G. Vlad, MD
Atrium Health Wake Forest Baptist
Outcome results
None listed