T81.4
Conditions
Interventions
Group 1: wound closure with a continuous subcuticular suture with a absorbable, monofile, non-coated suture (Monocryl 4x0)
Group 2: wound closure with an absorbable, monofile, triclosan-coated suture
Sponsors
Agaplesion Diakonieklinikum Rotenburg Wümme, Klinik für Allgemein-, Viszeral- und Thoraxchirurgie
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: planned laparotomy, elucidation
Exclusion criteria
Exclusion criteria: emergency, allergy to the suture, participation to a competing study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome is the occurrence of SSI defined by the CDC guidelines1 as superficial or deep incisional or either organ space infection. SSI is measured in incisional wounds after open abdominal surgery with skin suture with triclosan-coated poliglecaprone 25 (Monocryl plus; Ethicon GmbH, Norderstedt, Germany) in comparison with normal poliglecaprone 25 (Monocryl; Ethicon GmbH, Norderstedt, Germany) within 30 days after surgery | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary endpoints of this study are wound dehiscence and re-operation rate due to wound dehiscence, all-cause 30-day mortality and length of hospital stay. | — |
Countries
Germany
Contacts
Public ContactDaniel Matz
AGAPLESION Diakonieklinikum Rotenburg (Wümme)Klinik für Allgemein-, Viszeral- und Thoraxchirurgie
Outcome results
None listed