A Pilot Study to Assess the Efficacy of NEOX® CORD 1K® in the Treatment of Complex Diabetic Wounds

Johns Hopkins University

Status and phase: Withdrawn; Early Phase 1

Conditions: Diabetic Foot; Diabetic Foot Ulcer Mixed; Diabetic Foot Infection; Diabetic Foot Ulcer; Vascular Ulcer (Arterial or Venous Including Diabetic Ulcers Not Located on the Foot)

Treatments: Biological: NEOX® CORD 1K®

Study type: Interventional

Funder types: Other

Identifiers

NCT03296436

IRB00145403

Details and patient eligibility

About

Patients presenting to Johns Hopkins with a diabetic ulcer classified by the UT Grade 2 or 3 who meet all of the inclusion and none exclusion criteria and give their informed consent, will receive an application of NEOX CORD 1K in addition to standard of care procedures. Those patients will be seen in follow-up at weekly visits until the wound closes and epithelize, achieving complete closure. Subjects that do not achieve complete ulcer closure prior to or at the end of the 16 treatment weeks will exit the study.

Full description

A prospective investigator initiated trial will be conducted in diabetic patients with lower extremity wounds managed with NEOX CORD 1K umbilical cord product supplied by Amniox (a subsidiary of TissueTech, Inc.). The patient population will be comprised of Type 1 or Type 2 diabetics presenting to our hospital for the treatment of lower extremity wounds occurring on the dorsal and plantar foot. The wounds will be treated in the Operating Room (OR) arena including surgical debridement, resection of bone necrosis, biopsy, etc. to treat the associated morbidity. These wounds are classified utilizing the University of Texas (UT) Classification System as Grades: 2 (wounds penetrating to tendon or capsule) and 3 (wounds penetrating to bone or joint) with Stages: A (no infection or ischemia), B (Infection present), C (ischemia present) and D (Infection and ischemia present). This morbidity will comprise of complex wounds that exhibit exposed muscle, tendon, bone and may include the presence of treated osteomyelitis. This patient population oftentimes include diabetics with lower extremity ischemia or end stage renal disease and their associated comorbidities. These wounds are challenging in their care being they trend towards a poor prognosis including high morbidity and mortality as well as high major limb amputation rates. Hence, this trial will provide associated data to the efficacy of the above referenced material towards evaluating its effectiveness in these wound types towards enhancing wound healing and subsequently reducing amputation rates.

Sex: All

Ages: 18 to 100 years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

1. Male/female age 18 or older

2. Type 1 or Type 2 diabetes mellitus

3. Signed informed consent

4. Wound present for minimum for four (4) weeks

5. Wound location foot to include the dorsal or plantar surface

6. Serum creatinine < 3.0 mg/dL

7. HbA1c< 12% taken prior to randomization

8. Patient presents with adequate circulation to the effected extremity, as demonstrated

9. by one of the following within sixty (60) days:

10. Ankle-Brachial Index (ABI) with results of >0.6 and <1.2

11. Doppler arterial waveforms which are triphasic or biphasic at ankle of affected lower extremity

12. Wound is diabetic in origin with and area of > 1 cm2 and < 16 cm2 at time of screening

    Exclusion Criteria:

13. Unwilling to follow the visit requirements and instructions outlined by the protocol

14. Currently receiving radiation therapy or chemotherapy

15. Non-vascular surgical site

16. The subject's wound can be addressed by primary closure

17. Received growth factors, living skin, dermal substitutes, silver-containing products, amniotic membrane or umbilical cord products or other advanced biological therapies for wounds within 30 days of screening

18. Pregnant or breast feeding

19. HbA1c: > 12% within previous ninety (90) days

20. Serum creatinine level > 3.0 mg/dL Taking medications that are considered immune system modulators

21. Uncontrolled autoimmune surgical sites

22. Known or suspected local skin malignancy

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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0 participants in 1 patient group

Treatment Group

Experimental group

Description:

Group that will be receiving the investigational product

Treatment:

Biological: NEOX® CORD 1K®