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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03113747
Other study ID # MSC-P1
Secondary ID
Status Recruiting
Phase Phase 1/Phase 2
First received March 31, 2017
Last updated April 25, 2017
Start date March 25, 2015
Est. completion date December 26, 2018

Study information

Verified date April 2017
Source A.A. Partners, LLC
Contact Volodymyr S. Melnyk, MD, DSc
Phone +380679337461
Email V.Melnyk@ilaya.ua
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate safety and efficacy of tissue engineered construct based on allogeneic cultured adipose-derived multipotent mesenchymal stromal cells (ALLO-ADSCs) and platelet-poor plasma fibrin hydrogel to treat patients with 2-B and 3- degree burn wounds


Description:

For more than 20 years in clinical practice allogeneic transplantation of diploid fibroblasts (ADP) for burn wounds has been successfully used, it is used as an independent method, and a method of preparing wounds for autologous skin grafting [1].

The clinical efficacy of transplantation ADP, after the research done by E.V. Glushchenko; Rahayev AM [2,3] is not doubted.

Several studies have shown the efficacy of stem cells in promoting faster and superior wound healing. Alexaki [4] successfully used adipose derived mesenchymal stem cells in wound healing in mice and compared their effect with dermal fibroblasts. The application of stem cells in wounds promoted more efficient reepithelialization by their proliferative effect on keratinocytes.

In recent years, the world's leading burn centers attempted to restore the skin over large areas of burn wounds by epidermal layers transplantation of allogeneic cells cultured in culture medium.

The information expected in the study will be based on the principles of evidence-based medicine and will have practical significance for the treatment of burn wounds.

It is expected to show a positive effect of cultured multipotent mesenchymal stromal cells in the epithelization of burn wounds process as well as the extent and speed healing of skin flap during autologous skin grafting.


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date December 26, 2018
Est. primary completion date December 26, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Male and female aged 18-65 years;

- Patients with 2-nd B and 3-d degree burn wound;

- Body surface area involved in burns - from 10 to 50%;

- The area of skin grafting - less than 6% of the skin surface;

- Burn occurring within the 24 hours prior to the hospitalization;

- Adequate antishock therapy in the prehospital phase;

- Women of childbearing age to provide proof of a current, valid negative pregnancy test;

- Confirmation of participation in the study by signing the Instrument of Consent, personally or through a responsible caretaker.

Exclusion Criteria:

- Prognostically favorable or unfavorable outcome of the disease

- (Lesion Severity Index, less than 30 or more, than 120 score);

- Combined trauma;

- Severe respiratory tract burn injuries;

- Ischemic disease of the lower extremities;

- The presence of cardiovascular disease (CVD): symptoms of unstable angina, myocarditis, heart disease, heart failure;

- History of prior cancer;

- Healing of duodenal or gastric ulcers in history;

- Diabetes

- Severe chronic liver diseases or kidney disease in history;

- History of alcohol or other drug abuse;

- Pregnan?y;

- Any other physical diseases in decompensation or subcompensation,

- or those that are rated as severe or moderate;

- Therapeutic issues or psychiatric disorders of a patient which would

- make the subject unsuitable to participate in this study or to complete it;

- Participation in another clinical trial

Study Design


Related Conditions & MeSH terms


Intervention

Biological:
ALLO-ASCs
1). Cryopreserved cell suspension of early passages of cultured allogeneic MSCs isolated from SVF obtained from lipoaspirate, a total of 10 mln. of cultured cells; 2).The TE-construct consisting of collagen- or fibrin-derived hydrogels and cells of early passages (up to P5) suspension of allogeneic cultured MSCs isolated from SVF obtained from lipoaspirate; Biological is applied by surface application over perforated (1:3) autologous skin graft following the covering with hypoadhesive bandage. This procedure is carried out twice - once simultaneously with a skin grafting procedure and 2-3 days following autodermoplasty, while bandaging.

Locations

Country Name City State
Ukraine The Kyiv City Clinical Hospital ?2 Kyiv

Sponsors (1)

Lead Sponsor Collaborator
A.A. Partners, LLC

Country where clinical trial is conducted

Ukraine, 

References & Publications (1)

Alexaki VI, Simantiraki D, Panayiotopoulou M, Rasouli O, Venihaki M, Castana O, Alexakis D, Kampa M, Stathopoulos EN, Castanas E. Adipose tissue-derived mesenchymal cells support skin reepithelialization through secretion of KGF-1 and PDGF-BB: comparison with dermal fibroblasts. Cell Transplant. 2012;21(11):2441-54. doi: 10.3727/096368912X637064. Epub 2012 Apr 10. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary The degree of healing of skin flap; The degree of epithelialization of burn wounds in the perforations of a skin graft The degree of healing of skin flap after autologous skin grafting; up to 1 month
Secondary The dynamics of healing of skin flap Complete epithelization or epithelization more than 50% of the cells in the skin graft on the 10th day after autologous skin grafting are effective. The epithelialization less than 50% is not effective. up to 1 month
Secondary Dynamics of the phagocytic activity of neutrophils in the area of burn wounds, according to NBT-test. Dynamics of the phagocytic activity of neutrophils in the area of burn wounds, according to NBT-test. up to 1 month
Secondary Duration of treatment (days) to complete epithelialization of burn wounds; Duration of treatment (days) to complete epithelialization of burn wounds; up to 1 month