Adipose Derived Regenerative Cellular Therapy of Chronic Wounds

Diabetic Foot Clinical Trial

Official title:

Adipose Derived Regenerative Cellular Therapy of Chronic Wounds

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02092870
• Other study ID #: 001
• Status: Completed
• Phase: Phase 2
• Start date: September 2013
• Est. completion date: September 9, 2019

Study information

• Verified date: September 2019
• Source: Tower Outpatient Surgical Center
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Our study aims to explore the effects of Adipose Derived Stem Cells (ASCs) on chronic wounds.

Description:

In an attempt to explore the contribution of Adipose Derived Stem Cells (ASCs) to chronic wound healing, we will investigate the effects of injecting ASCs into the periphery and debrided surfaces of chronic wounds. Our goal is to achieve healing in two months, and for the wounds to stay healed for the following two weeks.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 25
• Est. completion date: September 9, 2019
• Est. primary completion date: September 2015
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Female or male patient aged = 18

• With diagnosis of diabetic or other chronic wound

• Grade 1 or 2 wound on the Wagner Scale

• Ulcer with a surface area comprised greater than 4 cm2 included (after mechanical debridement of the ulcer)

• For subjects with more than one wound that meet these criteria, all qualifying wounds may be treated

• Patient's wound has been refractory to standard of care (no measureable signs of healing for at least 30 days)

• Patient has adequate (>200cc) abdominal or other subcutaneous adipose tissue accessible by syringe-based lipoharvest

• Patient has activated platelet thromboplastin time (aPTT) of < 1.6x the mean normal reference interval at the time of the lipoharvest procedure and no contraindication to lipoharvest

Exclusion Criteria:

• Typical Charcot's foot

• Presence of osteitis (eq Br osteomyelitis) at the inclusion visit (evidenced with a radiological lesion facing the wound [bone erosion or disappearance of the cortical bone]) as determined by MRI

• Clinical evidence of uncontrolled infection at the inclusion visit

• Patient not eligible for syringe-based lipoharvest of at least 200cc of subcutaneous adipose tissue

• Subjects with cancerous or pre-cancerous lesions in the area to be treated

• Patient with working activity who cannot be on sick-leave during the study period

• Patient suffering from a psychiatric disorder not treated

• Clinical evidence of gangrene on any part of the affected foot

• Patient receiving corticosteroids, NSAIDs, immunosuppressive or cytotoxic agents, all systemic agents that can affect wound repair or any treatment that might interfere with the assessment of the study treatment

• Pregnant or nursing females

• Patient receiving dialysis for renal insufficiency or who have severe renal dysfunction

• Patient who cannot have an off-loading method

• Participation in any other clinical research study that has not reached the primary efficacy endpoint or otherwise would interfere with the patient's participation in this study

• Any concurrent disease or condition that, in the opinion of the investigator, would make the patient unsuitable for participation in the study

Related Conditions & MeSH terms

• Diabetic Foot
• Pressure Ulcer
• Ulcer
• Varicose Ulcer
• Venous Ulcer

Intervention

Drug:
• Adipose derived stem cells
ASCs harvested from autologous lipoaspirate

Locations

Country	Name	City	State
United States	Tower Outpatient Surgical Center	Los Angeles	California

Sponsors (1)

Lead Sponsor	Collaborator
Tower Outpatient Surgical Center

Country where clinical trial is conducted

United States, 

References & Publications (8)

Damour O, Gueugniaud PY, Berthin-Maghit M, Rousselle P, Berthod F, Sahuc F, Collombel C. A dermal substrate made of collagen--GAG--chitosan for deep burn coverage: first clinical uses. Clin Mater. 1994;15(4):273-6. — View Citation

Hanft JR, Surprenant MS. Healing of chronic foot ulcers in diabetic patients treated with a human fibroblast-derived dermis. J Foot Ankle Surg. 2002 Sep-Oct;41(5):291-9. — View Citation

King H, Aubert RE, Herman WH. Global burden of diabetes, 1995-2025: prevalence, numerical estimates, and projections. Diabetes Care. 1998 Sep;21(9):1414-31. — View Citation

Marston WA, Hanft J, Norwood P, Pollak R; Dermagraft Diabetic Foot Ulcer Study Group. The efficacy and safety of Dermagraft in improving the healing of chronic diabetic foot ulcers: results of a prospective randomized trial. Diabetes Care. 2003 Jun;26(6):1701-5. — View Citation

Reiber GE, Vileikyte L, Boyko EJ, del Aguila M, Smith DG, Lavery LA, Boulton AJ. Causal pathways for incident lower-extremity ulcers in patients with diabetes from two settings. Diabetes Care. 1999 Jan;22(1):157-62. — View Citation

Reiber GE. The epidemiology of diabetic foot problems. Diabet Med. 1996;13 Suppl 1:S6-11. Review. — View Citation

Wieman TJ, Smiell JM, Su Y. Efficacy and safety of a topical gel formulation of recombinant human platelet-derived growth factor-BB (becaplermin) in patients with chronic neuropathic diabetic ulcers. A phase III randomized placebo-controlled double-blind study. Diabetes Care. 1998 May;21(5):822-7. — View Citation

Williams R, Van Gaal L, Lucioni C; CODE-2 Advisory Board. Assessing the impact of complications on the costs of Type II diabetes. Diabetologia. 2002 Jul;45(7):S13-7. Epub 2002 Jun 12. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Percent change in wound size from baseline at 12 weeks		12 weeks

External Links

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