Clinical Evaluation of PoreSkin

Status Completed

Clinical Trial Summary

PoreSkin, a human acellular dermal matrix (hADM) manufactured by Faculty of Medicine, Chulalongkorn University, is the first human dermal substitute developed in Thailand. It is a permanent dermal substitute aiming to reduce skin contracture. The objective of this study is to assess the safety and ability in achieving durable and cosmetic coverage of PoreSkin.

Clinical Trial Description

n/a

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Treatment

Clinical Trial Details

NCT number	NCT02486874
Study type	Interventional
Source	Chulalongkorn University
Contact
Status	Completed
Phase	Phase 1
Start date	September 2009
Completion date	July 2010

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