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Effectiveness for Interventions to Minimize Surgical Site Infections

D

Dallas VA Medical Center

Status

Unknown

Conditions

Infections

Treatments

Procedure: Normal saline pressurized irrigation
Drug: sub-q gentamicin

Study type

Interventional

Funder types

Other U.S. Federal agency

Identifiers

NCT01153191
#10-046

Details and patient eligibility

About

The purpose of this study is to evaluate two different simple and inexpensive extra treatments during colorectal surgeries to see if this will reduce the rate of post operative infections

Full description

The population for inclusion for this study will be drawn from the patients undergoing elective transabdominal colorectal surgery. This population was chosen due to its inherently high rate of superficial-incisional infection.Colorectal procedures stand out as a particularly highrisk surgery with respect to SSI. Several studies have reported rates of infection of 25% or more making colorectal surgeries an excellent opportunity for testing new strategies to reduce SSI.

This pilot project seeks to preliminarily evaluate two new strategies that are inexpensive and could be readily incorporated into current practice. The strategies are pressurized irrigation of the superficial surgical wound (above the fascia) and subcutaneous injection of gentamicin into the surgical wound prior to initial skin incision. Comparison will be made between prospectively enrolled patients and historic controls.The hypothesis to be tested is that these interventions will significantly reduce superficial incisional infection rates compared with historic control.

Enrollment

120 estimated patients

Sex

All

Ages

18 to 95 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • VA patients getting transabdominal,elective colorectal procedures
  • willing and capable of giving self informed consent

Exclusion criteria

  • patients unable to give informed consent
  • emergency colorectal procedures
  • transanal procedures
  • patients who have contaminated or dirty wounds that would preclude attempts at skin closure at the conclusion of the procedure
  • patients undergoing appendectomy
  • patients undergoing intraabdominal procedures not including surgical resection of the colon or rectum (ie.procedures involving small bowel , stomach)
  • patients with pre/op creatinine clearance less than 20ml/min
  • patients with known allergy or hypersensitivity to gentamicin
  • patients that have received gentamicin within 2 weeks of potential study date

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

None (Open label)

120 participants in 2 patient groups

Pressurized irrigation
Experimental group
Description:
first group-After closure of patients abdominal wall fascia, Hydrostatic irrigation with 3 liters of normal saline with Simpulse Solo irrigation system (Davol) at less than 15PSI will be applied to subcutaneous tissues prior to closure
Treatment:
Procedure: Normal saline pressurized irrigation
Sub Q Antibiotic
Experimental group
Description:
second group of patients will receive 2mg/lg of gentamicin in 20 ml of sterile saline injected into the superficial tissues above the ABD wall fascia prior to initial incision
Treatment:
Drug: sub-q gentamicin

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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