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Effect of Triclosan-coated Suture on Superficial SSI

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02018289
Enrollment
106
Registered
2013-12-23
Start date
2007-10-31
Completion date
Unknown
Last updated
2013-12-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Surgical Site Infection

Keywords

Triclosan coated suture, Surgical site infection, Fecal peritonitis, Superficial, incisional

Brief summary

The abdominal closure with triclosan coated suture will reduce superficial surgical site infection.

Interventions

PROCEDURETriclosan coated suture

Suture of the abdominal wall with triclosan coated suture

PROCEDURENo triclosan

Suture of the abdominal wall with suture without triclosan coat

Sponsors

Hospital General Universitario Elche
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Fecal peritonitis

Exclusion criteria

* Perioperative mortality

Design outcomes

Primary

MeasureTime frameDescription
Superficial surgical site infection (SSI)60 postoperative daysSSI will be evaluated in the postoperative course and up to 60 days after surgery

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026