Status
Conditions
Treatments
About
Evaluation of safety and performance of the SPINNER device and wound dressing in the treatment of donor-site wounds (DSW)
Full description
The SPINNER is a hand held, portable electro-spinning device that produces personalized in-situ nanofiber dressings for the treatment of external burns and wounds.
The dressing has non-adherence, high absorbance, bacterial protection, easy and pain-free peel characteristics and shows excellent conformability and optimal coverage of the wound.
The objective of this study is to evaluate the safety and performance of the SPINNER device and wound dressing in the treatment of donor-site wounds (DSW) at size of 10-200 cm2.
The study will include five sites in Israel:
Sheba Medical Center, Tel Hashomer RambamMedical Center, Haifa Kaplan Medical Center, Rehovot Souraski Medical Center, Tel Aviv Beilinson Medical Center, Petach Tikva
Study primary endpoints:
Dermal Safety Wound healing and time to complete re-epithelialization at 1, 3, 5, 7, 14 and 21 days post operation
Study secondary endpoints:
Ease of use Pain assessment at 1, 3, 5, 7, 14 and 21 days post operation Infection assessment from 3 days post operation up to 21 days Device related adverse events of the SPINNER device and wound dressing
Extended exploratory follow up:
Assessment of itching and scarring from wound closure time and up to 12 months follow up
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
Exclusion criteria
Primary purpose
Allocation
Interventional model
Masking
41 participants in 2 patient groups
Loading...
Data sourced from clinicaltrials.gov
Clinical trials
Research sites
Resources
Legal