PMCF-study Using Novosyn® Quick Suture Material for Skin Closure (SKINNOQ)

Aesculap

Status: Completed

Conditions: Skin Closure

Treatments: Device: Novosyn® Quick

Study type: Observational

Funder types: Industry

Identifiers

NCT02680886

AAG-O-H-1505

Details and patient eligibility

About

The aim of this study is to show that the performance of Novosyn® Quick suture material is comparable with other suture material used for skin closure. In order to show that, various safety and efficacy parameters have been selected. The outcome regarding these parameters will be evaluated by a quantitative summary of the available clinical data from the literature.

Enrollment: 100 patients

Sex: All

Ages: 1+ year old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Pediatric and adult patients undergoing skin closure
• Small linear minimally contaminated incision / lacerations on the trunk or extremities
• Written informed consent

Exclusion criteria

• Emergency surgery
• Facial lacerations or incisions
• Visible dirt in the wounds
• Nonlinear shape
• Patients taking medical consumption that might affect wound healing

Trial design

100 participants in 1 patient group

Novosyn® Quick

Description:

Skin closure using rapid absorbable suture material

Treatment:

Device: Novosyn® Quick