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Terminated Not applicable Interventional Results available

Irrisept Versus Standard of Care in the Prevention of Surgical Site Infections

ClinicalTrials.gov ID: NCT02255487

Public ClinicalTrials.gov record NCT02255487. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 17, 2026, 7:39 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase IV, Multicenter, Prospective, Randomized, Controlled Clinical Study to Compare the Irrisept System Versus Standard of Care (SoC) on the Prevalence of Surgical Site Infections in Patients With Abdominal Trauma or Acute Surgical Abdomen

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study was to compare the rate of surgical site infections in patients randomized to Irrisept versus SoC, who had an open abdominal laparotomy for abdominal trauma or acute surgical abdomen.

Study identification

NCT ID
NCT02255487
Recruitment status
Terminated
Study type
Interventional
Phase
Not applicable
Lead sponsor
Irrimax Corporation
Industry
Enrollment
627 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 18, 2015 (Actual)
Primary completion
Mar 13, 2017 (Actual)
Completion
Mar 13, 2017 (Actual)
Last update posted
May 24, 2022

2015 – 2017

United States locations

U.S. sites
17
U.S. states
14
U.S. cities
17
Facility City State ZIP Site status
The University of Arizona Tucson Arizona 85724 —
The University of Southern California, USC Medical Center Los Angeles California 90033 —
Denver Health and Hospital Authority Denver Colorado 80204 —
The University of South Florida, Tampa General Hospital Tampa Florida 33606 —
The University of Iowa Iowa City Iowa 52242 —
The University of Kentucky Research Foundation Lexington Kentucky 40536 —
The University of Maryland, Baltimore Baltimore Maryland 21201 —
Baystate Medical Center Springfield Massachusetts 01199 —
Saint Louis University St Louis Missouri 63110 —
The University of Cincinnati Health Cincinnati Ohio 45267 —
The MetroHealth System Cleveland Ohio 73160 —
Regional One Health Research Institute Memphis Tennessee 38163 —
The University of Texas Southwestern Medical Center Dallas Texas 75390 —
The University of Texas Health Science Center at Houston Houston Texas 77030 —
The University of Texas Health Science Center at San Antonio San Antonio Texas 78229 —
The University of Washington, Harborview Medical Center Seattle Washington 98104 —
The Medical College of Wisconsin Milwaukee Wisconsin 53226 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02255487, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 24, 2022 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02255487 live on ClinicalTrials.gov.

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