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Scar Formation clinical trials

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NCT ID: NCT01750424 Withdrawn - Clinical trials for Autologous Fat Grafting

3-D Imaging Assessment of Scar Formation and Would Healing in Fat Grafted vs Non-Fat Grafted Facial Reconstruction Wound Sites

Start date: November 2012
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to assess scar-formation and wound healing following the use of autologous fat grafting in facial reconstruction patients. Patients who have undergone facial reconstruction in the last 3 months will be randomized into two groups, one receiving fat grafting and one not receiving any intervention. These patients will continue to follow-up in our clinic for one year, with 3-D images taken at each follow-up visit to assess scar formation and wound healing. Assessment of the scar will be undertaken by both healthcare personnel as well as general lay public. We hypothesize that patients undergoing fat grafting to the wound site will achieve a more aesthetically appealing result, with less scarring and improved wound healing as judged by both the general public and healthcare professionals.

NCT ID: NCT01454310 Completed - Wound Healing Clinical Trials

An Acellular Epithelial Skin Substitute in Deep Partial-thickness Burns

Start date: November 2010
Phase: Phase 4
Study type: Interventional

The purpose of the study is to compare an acellular epithelial skin substitute with autologous split-thickness skin grafts (STSGs) in deep partial-thickness burns. The objective is to evaluate skin quality and scar formation by using subjective and objective burn scar assessments in order to present valuable data for another additional option of wound coverage in deep partial-thickness burns. The investigators hypothesized that the acellular epithelial skin substitute is at least not inferior to autologous skin grafts.

NCT ID: NCT01053897 Completed - Scar Formation Clinical Trials

Study of GBT009 for Treatment of Incisional Wounds Following Breast Reconstruction Surgery

Start date: January 2010
Phase: Phase 2
Study type: Interventional

The primary objective of this study is to assess whether intradermal injections of GBT009 along full thickness incisions following surgery results in an improvement in scar appearance.