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

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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

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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