SNaP Wound Care System Over Skin Cancer Excision Sites and Split Thickness Skin Grafts (STSGs)

Solventum US LLC

Status: Withdrawn

Conditions: Split Thickness Skin Graft; Skin Graft; Skin Cancer Excision Site

Treatments: Device: SNaP® Wound Care System

Study type: Observational

Funder types: Industry

Identifiers

NCT01349894

011111

Details and patient eligibility

About

The purpose of this study is to evaluate the efficacy of the Spiracur SNaP® Wound Care System for the treatment of skin cancer excision sites and split thickness skin grafts (STSG). The secondary purpose will be to compare the prospective patients to retrospectively treated skin cancer excision sites and STSGs to further evaluate efficacy and safety.

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Skin cancer excision site and/or STSG as the source of the wound on any part of the body including head and neck, torso, and extremities. Any other type of skin graft will also be eligible for inclusion into the study.
• Wound < 16 cm in greatest diameter
• Subject ≥ 18 years of age
• Female subjects of child-bearing potential must be willing to take a urine pregnancy test prior to starting study
• Subject is willing and able to sign informed consent

Exclusion criteria

• Wound-related cellulitis
• Wound located in an area not amenable to forming an air-tight seal
• Subject has untreated osteomyelitis
• Subject is allergic to wound care products
• Wound has exposed blood vessels not suitable for negative pressure therapy
• Subject is actively participating in other clinical trials that conflict with current study
• Subject has fistulas
• Subject is pregnant

Trial design

0 participants in 1 patient group

SNaP® Wound Care System

Treatment:

Device: SNaP® Wound Care System