The skin plays a critical role in protection where it acts as a barrier from damage and pathogens between the external and internal environments. Wounds compromise its protective role by disrupting the function and the normal structure of the skin and the underlying soft tissue. As a response to injury wound healing occurs in order to rapidly restore the defect. This process involves activation of keratinocytes, fibroblasts, endothelial cells, macrophages, and platelets and consists of multiple phases including hemostasis, inflammation, migration and cellular proliferation, and maturation and remodeling. A simplified schematic of the course of wound healing is depicted in Figure 2. Hemostasis occurs immediately after dermal injury. The inflammation phase is characterized by cellular recruitment and increased vascular permeability. The epithelization phase is achieved by proliferation of basal cells and migration of epithelial cells. The last phase is known as the maturation and remodeling phase where collagen cross-linking and remodeling, wound contraction, and repigmentation takes place. Due to the broad involvement of various cell types, extracellular matrix and many reactive molecules each phase in wound healing produces characteristic changes within the tissue. A deficiency in any part of the process can lead to delayed wound healing, abnormal scar formation or chronic wounds. To study wound healing in healthy volunteers a challenge model with skin punch biopsies has been described in literature previously. However, the characterization of this model was not performed comprehensively since advanced analysis of biopsies were omitted. Furthermore, analyses performed in previous studies only partially described wound healing processes either by insufficient time points for characterization or scarce simultaneous evaluations of multiple wound healing modalities. The overall aim of this study is to develop a standardized model to temporarily and locally induce a skin trauma to investigate wound healing and monitor wound closure. This clinical model will enable future application as proof-of-pharmacology and proof-of concept studies as well as drug profiling in early drug development programs. More specifically, the objective of the trial is to explore and characterize the induction of well-defined skin trauma and natural wound healing process over the course of the different phases using a battery of dermatological assessments after skin punch biopsies in healthy volunteers. Furthermore, safety and tolerability will be assessed. Characterization and monitoring of wound healing effects following skin punch biopsies will be performed by means of biophysical, biochemical, imaging, clinical parameters and subject reported outcomes.
Age range
18 Years – 30 Years
Sex
ALL
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Biopsy biomarkers
Timeframe: 3 months after end of study
Local skin biomarkers
Timeframe: 3 months after end of study
Clinical imaging
Timeframe: 3 months after end of study
Clinical evaluation
Timeframe: 3 months after end of study
Skin microbiome
Timeframe: 3 months after end of study
Biopsy biomarkers
Timeframe: 3 months after end of study
Biopsy biomarkers
Timeframe: 3 months after end of study
Clinical imaging
Timeframe: 3 months after end of study
Clinical imaging
Timeframe: 3 months after end of study
Clinical imaging
Timeframe: 3 months after end of study
Clinical imaging
Timeframe: 3 months after end of study
Clinical imaging
Timeframe: 3 months after end of study
Clinical evaluation
Timeframe: 3 months after end of study
Clinical evaluation
Timeframe: 3 months after end of study