drugset / Trial / NCT05335720
Efficacy and Safety Evaluation of EASYEF® in Acute Wound (Split-thickness Skin Graft Donor Site)
RandomizedParallel-groupOpen-labelTreatment
Summary
This study is a prospective study, randomized, using control, open-label, single-center to evaluate the efficacy and safety of EASYEF® in acute wound (split-thickness skin graft donor site). A total of 10 subjects are randomly allocated. Subjects who meet the final inclusion and exclusion criteria are randomized to the test cohorts in a ratio of 1:1:1.
Timeline
- Start
- 2019-07-19
- Primary completion
- 2020-03-01
- Completion
- 2020-04-08
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | NEPIDERMIN | Protein / enzyme biologic | 50 ug | Topical |
Indications
No indication recorded.