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Total Occlusive Ionic Silver-containing Dressing vs Mupirocin Ointment Application vs Conventional Dressing in Elective Colorectal Surgery: Effect on Incisional Surgical Site Infection

H

Hospital General Universitario Elche

Status and phase

Completed
Phase 3

Conditions

Incisional Surgical Site Infections

Treatments

Procedure: ionic silver-containing dressing
Procedure: Mupirocin ointment application

Study type

Interventional

Funder types

Other

Identifiers

NCT02267122
Hospital General Elche

Details and patient eligibility

About

The patients were randomized into 3 groups: those patients undergoing a ionic silver-containing dressing (ISD) (Group 1), those undergoing a Mupirocin ointment application (MOA) (Group 2) and those using a conventional dressing (Group 3) in the surgical wound after finishing an elective colorectal surgery.

Enrollment

147 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosis of colorectal neoplasms and plans to undergo an elective surgery with curative aims.
  • Open surgical approach

Exclusion criteria

  • Anastomotic leak
  • Mortality
  • Lost to follow-up

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

147 participants in 3 patient groups

ionic silver-containing dressing
Experimental group
Description:
After placing the staples, a ionic silver-containing dressing was placed covering the wound.
Treatment:
Procedure: ionic silver-containing dressing
Mupirocin ointment application
Experimental group
Description:
After placing the staples, a Mupirocin ointment application was placed covering the wound.
Treatment:
Procedure: Mupirocin ointment application
Conventional dressing
No Intervention group
Description:
After placing the staples, a conventional dressing, without application of any special gauze or ointment, was placed covering the wound

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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