Bioengineered Skin and Wound Healing
Primary Purpose
Leg Ulcers
Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Bioengineered skin
Sponsored by
About this trial
This is an interventional treatment trial for Leg Ulcers focused on measuring Bioengineered skin, Venous leg ulcer
Eligibility Criteria
Inclusion Criteria: Men or women at least 18 years old At least one ulcer (wound) greater than or equal to 2 centimeters Ulcer (wound) present for at least 3 months or greater Ankle/brachial index > 0.7 Patient must be ambulatory Patient must read, understand and sign informed consent Exclusion Criteria: Medical conditions limiting participation History of poor compliance, unreliability History of allergy to bovine collagen Gangrene, vasculitis, collagen vascular disease osteomyelitis or exposed tendons Use of systemic steroids/immunosuppressives History of diabetes mellitus
Sites / Locations
- Roger Williams Medical Center Dept. of Dermatology & Skin Surgery
Outcomes
Primary Outcome Measures
Measurement and characterization of stimulation of the wound's edges treated with the bioengineered skin construct (BSC)
Secondary Outcome Measures
Response of BSC to injury, including meshed (wounded) and unmeshed BSC
Activation of certain critical cytokines, including IL-1 alpha, IL-6, and TGF-beta
Full Information
NCT ID
NCT00007280
First Posted
December 16, 2000
Last Updated
August 1, 2013
Sponsor
Roger Williams Medical Center
Collaborators
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
1. Study Identification
Unique Protocol Identification Number
NCT00007280
Brief Title
Bioengineered Skin and Wound Healing
Official Title
Mechanisms of Bioengineered Skin in Human Wounds
Study Type
Interventional
2. Study Status
Record Verification Date
April 2008
Overall Recruitment Status
Completed
Study Start Date
October 2000 (undefined)
Primary Completion Date
August 2005 (Actual)
Study Completion Date
August 2005 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Roger Williams Medical Center
Collaborators
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
4. Oversight
5. Study Description
Brief Summary
This study will look at whether a graft of bioengineered skin (BSC), known commercially as Apligraf, stimulates the healing process in a person's own skin at the edge of a wound (known as the edge effect). The information from this study will provide a better understanding of the ways that grafts of bioengineered skin help the healing of chronic wounds.
We will assign study participants to either the bioengineered skin group or the control group. People in the control group will receive compression therapy with a multilayered compression bandage. We will examine each participant before starting treatment and then once a week for 24 weeks or until the wound heals. On the first day of treatment (day 0) and at week 3, week 6, and week 24 (end of treatment) we will take a small tissue sample from the wound for a biopsy. After the wound is completely healed, we will ask the patient to return once a month for 6 months to make sure the wound stays healed.
Detailed Description
BSC is a two-layered sheet made from purified beef tendon collagen, living human cells, and a substance that maintains the cells until they are grafted (removed). We will obtain human cells from donors unrelated to the patient. The human cells have been tested for the presence of infectious agents and found to be free of disease-causing organisms such as hepatitis virus, the AIDS virus, bacteria, and fungi.
We will randomly assign (randomize) study participants to either the bioengineered skin group or control group (compression therapy with a multilayered compression bandage). Regardless of the group to which a patient is assigned, we expect participation in this study for 12 months following the start of study treatment. We will examine each patient at the screening visit (2 weeks before randomization) and then again 3-4 days before the start of treatment to make sure the wound is free of any signs of infection. After the initial randomization visit we will examine the wound once a week for 24 weeks or until the wound heals, whichever is earlier. As soon as we have determined that the wound is completely healed, we will ask the patient to return once a month for 6 months to make sure it remains healed.
Bioengineered skin group: We will apply BSC to the wound and cover it with xeroform dressing, foam bolster, gauze dressing, and compression bandage. If we do not note any improvement at the week 6 visit, we will apply BSC on the wound a second time.
Control group: We will place a multilayered compression bandage on the wound of participants assigned to this group.
Biopsies (small piece of skin tissue): At day 0 a biopsy will be taken from the thigh and leg ulcer. The biopsy from the thigh will require sutures and will be removed in ten days. Sometime between weeks 1 and 3, week 6, week 24 and week 48 (6 month follow-up) visits a biopsy will be taken from the ulcer (wound) if the ulcer has not healed. If the ulcer is healed at the week 48 visit, a light scraping of the healed wound will be performed.
Study examinations: All study examinations will include observation, measurement, and photography.
We can only admit women of childbearing age to the study if they are not breast feeding, not pregnant, or have been surgically sterilized or are using effective birth control. Because the effects of the proposed treatments on a fetus are unknown, we will remove from the study any woman who becomes pregnant while receiving BSC applications (day 0-week 3) and suggest another method of treatment.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Leg Ulcers
Keywords
Bioengineered skin, Venous leg ulcer
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
50 (Actual)
8. Arms, Groups, and Interventions
Intervention Type
Device
Intervention Name(s)
Bioengineered skin
Primary Outcome Measure Information:
Title
Measurement and characterization of stimulation of the wound's edges treated with the bioengineered skin construct (BSC)
Time Frame
Measured throughout the study till Week 48
Secondary Outcome Measure Information:
Title
Response of BSC to injury, including meshed (wounded) and unmeshed BSC
Time Frame
Measured throughout the study till Week 48
Title
Activation of certain critical cytokines, including IL-1 alpha, IL-6, and TGF-beta
Time Frame
Measured throughout the study till Week 48
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Men or women at least 18 years old
At least one ulcer (wound) greater than or equal to 2 centimeters
Ulcer (wound) present for at least 3 months or greater
Ankle/brachial index > 0.7
Patient must be ambulatory
Patient must read, understand and sign informed consent
Exclusion Criteria:
Medical conditions limiting participation
History of poor compliance, unreliability
History of allergy to bovine collagen
Gangrene, vasculitis, collagen vascular disease osteomyelitis or exposed tendons
Use of systemic steroids/immunosuppressives
History of diabetes mellitus
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Vincent Falanga, MD
Organizational Affiliation
Roger Williams Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Roger Williams Medical Center Dept. of Dermatology & Skin Surgery
City
Providence
State/Province
Rhode Island
ZIP/Postal Code
02908
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
10781211
Citation
Falanga V, Sabolinski M. A bilayered living skin construct (APLIGRAF) accelerates complete closure of hard-to-heal venous ulcers. Wound Repair Regen. 1999 Jul-Aug;7(4):201-7. doi: 10.1046/j.1524-475x.1999.00201.x.
Results Reference
background
PubMed Identifier
12230509
Citation
Falanga V, Isaacs C, Paquette D, Downing G, Kouttab N, Butmarc J, Badiavas E, Hardin-Young J. Wounding of bioengineered skin: cellular and molecular aspects after injury. J Invest Dermatol. 2002 Sep;119(3):653-60. doi: 10.1046/j.1523-1747.2002.01865.x.
Results Reference
background
PubMed Identifier
11858954
Citation
Nahm WK, Zhou L, Falanga V. Sustained ability for fibroblast outgrowth from stored neonatal foreskin: a model for studying mechanisms of fibroblast outgrowth. J Dermatol Sci. 2002 Feb;28(2):152-8. doi: 10.1016/s0923-1811(01)00157-8.
Results Reference
background
PubMed Identifier
12164746
Citation
Phillips TJ, Manzoor J, Rojas A, Isaacs C, Carson P, Sabolinski M, Young J, Falanga V. The longevity of a bilayered skin substitute after application to venous ulcers. Arch Dermatol. 2002 Aug;138(8):1079-81. doi: 10.1001/archderm.138.8.1079.
Results Reference
background
PubMed Identifier
12707099
Citation
Badiavas EV, Falanga V. Treatment of chronic wounds with bone marrow-derived cells. Arch Dermatol. 2003 Apr;139(4):510-6. doi: 10.1001/archderm.139.4.510.
Results Reference
background
PubMed Identifier
12704642
Citation
Kim BC, Kim HT, Park SH, Cha JS, Yufit T, Kim SJ, Falanga V. Fibroblasts from chronic wounds show altered TGF-beta-signaling and decreased TGF-beta Type II receptor expression. J Cell Physiol. 2003 Jun;195(3):331-6. doi: 10.1002/jcp.10301.
Results Reference
background
PubMed Identifier
12598704
Citation
Shen JT, Falanga V. Growth factors, signal transduction, and cellular responses. J Dermatol. 2003 Jan;30(1):5-16.
Results Reference
background
PubMed Identifier
15174101
Citation
Nahm WK, Philpot BD, Adams MM, Badiavas EV, Zhou LH, Butmarc J, Bear MF, Falanga V. Significance of N-methyl-D-aspartate (NMDA) receptor-mediated signaling in human keratinocytes. J Cell Physiol. 2004 Aug;200(2):309-17. doi: 10.1002/jcp.20010.
Results Reference
background
PubMed Identifier
15223495
Citation
Brem H, Kirsner RS, Falanga V. Protocol for the successful treatment of venous ulcers. Am J Surg. 2004 Jul;188(1A Suppl):1-8. doi: 10.1016/S0002-9610(03)00284-8.
Results Reference
background
PubMed Identifier
15274699
Citation
Saap LJ, Donohue K, Falanga V. Clinical classification of bioengineered skin use and its correlation with healing of diabetic and venous ulcers. Dermatol Surg. 2004 Aug;30(8):1095-100. doi: 10.1111/j.1524-4725.2004.30334.x.
Results Reference
background
PubMed Identifier
15260809
Citation
Butmarc J, Yufit T, Carson P, Falanga V. Human beta-defensin-2 expression is increased in chronic wounds. Wound Repair Regen. 2004 Jul-Aug;12(4):439-43. doi: 10.1111/j.1067-1927.2004.12405.x.
Results Reference
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Bioengineered Skin and Wound Healing
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