Clinical Trials

Researchers are performing this study to evaluate if intraoperative angiography can be shown numerically to determine which wounds are at high risk of wound necrosis/breakdown.

The purpose of this study is to evaluate the safety of PEP in skin graft wounds.

The purpose of this study is to determine whether an increased dose closer to surgery of this oral nutritional supplement PCA can result in a change in C. acnes positive cultures and bacterial load seen at the time of elective primary Total Shoulder Arthroplasty (TSA). We seek to determine whether this higher dose of the nutrient supplement changes the bacterial load during total shoulder arthroplasty. Our hypothesis is that subjects who consume the increased dose of the nutrient supplement may exhibit a reduction the growth of C. acnes, especially in the deeper cultures.

The purpose of this study is to evaluate the effectiveness of Vacuum-assisted dressings for treating patients who have open chest wounds by comparing the time-to-closure of such wounds to traditional wound care management.

The purpose of this study is to determine feasibility of Kerecis intact fish skin for healing of fistula-in-ano and associated non-healing draining wounds.

The purpose of this study is to evaluate the safety and effectiveness of Adherus Dural Sealant when used in conjunction with standard methods of dural repair in spinal procedures. This trial uses the commercially available DuraSeal Exact (P080013b) as an active control. The trial is designed to demonstrate non-inferiority of Adherus Dural Sealant to DuraSeal Exact.
Subjects who have consented to participate in this study prior to undergoing spinal surgery and experience a durotomy, will be considered for study enrollment.
 

The purpose of this study is to assess wound perfusion at the site of closure in primary spine surgery between running subcuticular suture, interrupted vertical mattress suture, and staple closure techniques.