Study to Assess the Safety and Efficacy of DERMASEAL for the Treatment of Split-Thickness Skin Gr… (NCT06134843) | Clinical Trial Compass
Not Yet RecruitingPhase 1/2
Study to Assess the Safety and Efficacy of DERMASEAL for the Treatment of Split-Thickness Skin Graft Donor Site Wounds
12 participantsStarted 2024-09-01
Plain-language summary
The goal of this study to determine whether the combination biologic/drug DERMASEAL will safely decrease donor wound pain after split-thickness skin graft surgery. Participants will have their skin graft donor sites immediately treated with DERMASEAL versus standard of care wound dressings followed by periodic monitoring of their recovery.
Who can participate
Age range21 Years
SexALL
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Inclusion criteria
✓. Men or women ≥ 21 years of age.
✓. The subject is able and willing to adhere to study procedures and informed consent is obtained.
✓. Patient scheduled to undergo a split-thickness skin graft \> 25 cm2 and ≤ 300 cm2 with a wound depth of between 0.010 - 0.015 inch (0.2 - 0.4 mm).
✓. Target donor site wound involving the torso or upper or lower extremities.
✓. Patient has a palpable pulse at the wrist or ankle indicating adequate arterial perfusion of the extremity from which the skin graft is harvested.
✓. Serum creatinine \<2.0 mg/dl within the last 6 months.
✓. Negative urine pregnancy test at screening for women of childbearing potential. i) Women participants are considered of non-childbearing potential if they are pre-menopausal with a documented hysterectomy or bilateral oophorectomy; or post-menopausal defined as the cessation of regular menses for at least 12 consecutive months with no alternative pathological or physiological cause; or have a serum FSH level confirming the post-menopausal state.
Exclusion criteria
✕. Hypersensitivity to silver or fresh frozen plasma.
✕. Active infection or history of radiation to the donor site.
. The subject was previously entered into this study or had participated in any study drug or medical device study within 30 days of screening.
✕. Currently on a treatment regimen or medications which in the opinion of the investigator are known to interfere with wound healing (for example: cancer chemotherapy or equivalent immunosuppressants, systemic steroids \> 10 days of treatment, cytostatic drugs, COX-2 inhibitors, or radiation therapy).
✕. Excessive lymphedema that in the opinion of the investigator will interfere with wound healing.
✕. A cognitive, physical, or psychological condition interfering with subject's ability to comply with the treatment regimen.