Clinical Trials Logo

Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05517902
Other study ID # MNK15011001
Secondary ID
Status Active, not recruiting
Phase Phase 3
First received
Last updated
Start date April 28, 2023
Est. completion date May 30, 2024

Study information

Verified date May 2024
Source Mallinckrodt
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Autografting is a surgical procedure to transplant healthy skin (donor skin) from another part of the participant's own body (donor site) to the burned part. Autografting is the usual treatment for DPT burns. It works to close the wound, but can cause other problems: - Donor sites are painful, can become infected or scarred, or can even become full thickness (FT) wounds themselves - Treatment problems can require more grafting - Additional surgery increases the risk of medical problems caused by the treatment Stratatech is trying to find a safe and effective alternative to autografting to promote the healing of severe burns. The purpose of this study is to evaluate whether StrataGraft treatment eliminates or reduces the need for autografting and promotes wound closure in a pediatric population with thermal burns that contain intact dermal elements and for which autografting is clinically indicated (DPT burns). Participants will be enrolled into one of two age-based cohorts: 2 to < 12 years and 12 to ≤ 17 years to receive a single application of StrataGraft, in up to 3 non-contiguous DPT burn areas located on the same extremity or plane of the torso. The study will last for approximately 2.5 years.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 1
Est. completion date May 30, 2024
Est. primary completion date May 30, 2024
Accepts healthy volunteers No
Gender All
Age group 2 Years to 17 Years
Eligibility Inclusion Criteria: - Written informed consent provided by the parent(s) or legal guardian(s) and assent from the child when appropriate - Have enough healthy skin to reserve as donor site(s), in case autografting becomes necessary - Thermal burns of no more than a total of 30% TBSA - Study treatment sites that are DPT in depth and which are clinically indicated for excision and autografting, and located on the torso or extremities - Study treatment area(s) totaling 0.5% to 10% TBSA and may be composed of up to 3 non-contiguous areas located on the same extremity or plane of the torso - Sufficient healthy skin available and reserved as a donor site in the event that the StrataGraft treatment site requires autografting Exclusion Criteria: - Is pregnant or breastfeeding - Receiving treatment to suppress the immune system and/or systemic corticosteroids (inhaled corticosteroids are permitted) - A known history of malignancy - Pre-admission insulin-dependent diabetes - Concurrent trauma, conditions, and/or personal situations that, in the opinion of the investigator, may compromise the participant's safety or the study objectives - A burn injury that occurred = 14 days prior to planned StrataGraft application Is expected to survive less than 12 months - Is participating in another interventional trial, or did within 90 days before enrollment - A proposed study treatment site that has been previously excised or autografted; located adjacent to an undebrided/unexcised burn area; demonstrates signs and symptoms of wound infection, per judgement of the clinical investigator; lies across joints or is located on the feet (i.e., distal to the malleolus), hands (distal to the wrist), face, neck, buttocks, perineum, or genitalia

Study Design


Related Conditions & MeSH terms


Intervention

Biological:
StrataGraft
StrataGraft® Construct

Locations

Country Name City State
United States University of Wisconsin-Madison Madison Wisconsin

Sponsors (2)

Lead Sponsor Collaborator
Stratatech, a Mallinckrodt Company Biomedical Advanced Research and Development Authority

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Percentage of Participants Achieving Confirmed Complete Closure of StrataGraft Treatment Sites without Autograft within 12 Weeks of StrataGraft Application Confirmed complete wound closure is defined as complete skin re-epithelialization of the wound without drainage observed at 2 consecutive visits at least 2 weeks apart, but no later than Week 20. Up to 12 weeks
Primary Number of Participants With Treatment-emergent Adverse Events (TEAEs) An Adverse Event (AE) is any untoward or undesirable medical occurrence in a participant who is administered a study treatment and considered to be related to StrataGraft. TEAEs are defined as those that are not present at start of study treatment or that represent the exacerbation of a pre-existing condition during the treatment-emergent period. The treatment-emergent period is defined as the time from first application of StrataGraft to the end of the study for each participant. Up to 12 months
Secondary Mean Percent Area of StrataGraft Treatment Sites per Participant Closed at Week 12 Without Autograft Placement The mean percent area of StrataGraft treatment site closed at Week 12 without autograft placement will be calculated using the percent of the total treatment site re-epithelialized without autografting at Week 12. Week 12
Secondary Mean Percent Area of StrataGraft Treatment Sites per Participant Autografted by Week 12 The percent of the total treatment site area autografted will be calculated by using the percent of the total treatment site as the denominator and the area grafted as the numerator to calculate the percentage of the treatment site grafted. Week 12
Secondary Number of Confirmed Complete Wound Closures of the Strata Graft Treatment Sites on or Before Week 12 Without Autograft Placement Up to Week 12
See also
  Status Clinical Trial Phase
Completed NCT05023135 - DeepView SnapShot Portable (DV-SSP): Device Training Study
Completed NCT05276869 - Reliability and Feasibility of WeeFIM Instrument to Measure Functional Independence in Pediatric Burns
Completed NCT04548635 - VR for Burn Dressing Changes at Home Phase 2/Phase 3
Not yet recruiting NCT06076031 - Effects of Applying Streaming Media on Reducing Pain in Patient With Second-degree Burn During Changing Dressing N/A
Recruiting NCT05084248 - Vitamin D Deficiency in Adults Following a Major Burn Injury Phase 4
Completed NCT03113253 - TRANexamic Acid to Reduce Bleeding in BURN Surgery Phase 4
Recruiting NCT04090424 - Assessment of Safety and Effectiveness of NovoSorb® BTM in Severe Burns N/A
Not yet recruiting NCT05649891 - Checklists Resuscitation Emergency Department N/A
Withdrawn NCT03159182 - Study of Silicone Material Inserts To Treat Burn Scars N/A
Recruiting NCT02904941 - Human Amniotic Versus Synthetic Membrane as a Transient Skin Cover for Pediatric Burns N/A
Completed NCT02681757 - Comparison of Mepitel Ag vs Antibiotic Ointment Used With Soft Cast Technique for Treatment of Pediatric Burns N/A
Recruiting NCT01812941 - Evaluation of Mitochondrial Dysfunction in Severe Burn and Trauma Patients N/A
Completed NCT01437852 - StrataGraft® Skin Tissue as an Alternative to Autografting Deep Partial-Thickness Burns Phase 1
Completed NCT01214811 - Open Multi-centre Investigation to Evaluate Signs and Symptoms of Local Inflammation/Infection on Chronic Ulcers and Partial Thickness Burns When Using Mepilex Border Ag as an Anti-microbial Wound Dressing Phase 3
Completed NCT01061502 - Efficacy Study of a Bioelectric Dressing to Treat Skin Graft Donor Site Wounds Phase 1/Phase 2
Terminated NCT00822796 - Thermogard™ Efficacy Trial N/A
Terminated NCT00634166 - Effects of Therapy With Sulfamylon® 5% Topical Solution Compared to a Historical Control Group Phase 4
Terminated NCT00824681 - Effect of Music Therapy on Families of Burn Patients Phase 1
Terminated NCT00464386 - Continuous Glucose Monitoring (POC) in the ICU N/A
Withdrawn NCT00216983 - Proline Metabolism in Severely Burned Patients: Effect of Modulated Parenteral Feeding N/A