Clinical Trials Directory

Trials / Completed

CompletedNCT00353613

Prevention of Surgical Site Infections

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
900 (actual)
Sponsor
The University of Texas Health Science Center, Houston · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The primary research question is whether interventions to prevent caregiver and system errors will increase the proportion of laparotomy patients who receive recommended measures to prevent surgical site infections.

Detailed description

Background: Surgical site infections (SSIs) cause significant and largely preventable morbidity, mortality, and resource use due to failure to comply with evidence-based guidelines. Quality improvement programs report increased compliance with these guidelines, but are subject to a variety of biases. Hypothesis: The primary hypothesis is that a targeted intervention program will increase the proportion of patients in a county hospital who receive recommended interventions to prevent SSIs, when assessed in the most rigorous feasible clinical trial. The specific aims of the trial are to establish practical surveillance measures to determine the percentage of patients whose care complies with 5 major guidelines to prevent SSIs; to use chart review, direct observation, attitude surveys, and focus groups to identify, quantify, and address latent and active errors linked to non-compliance, and to develop, implement, and assess the effectiveness of an intervention program to increase guideline compliance. Study Design: An innovative trial design will be performed with 3 staggered phases in the two major county hospitals in Houston, TX. This design allows for adjustment for temporal trends and hospital differences in assessing the intervention program in a large, high-risk, disadvantaged urban population. Based on a compliance goal of 95%, this design has adequate power to detect even a small absolute increase ( \>= 5%) above baseline in the percentage of patients receiving all 5 recommended preventive measures.

Conditions

Interventions

TypeNameDescription
BEHAVIORALPackage of targeted interventions to reduce errorInterventions will include changes in administration of antibiotics and the improved monitoring of blood glucose and body temperature peri-operatively.

Timeline

Start date
2007-03-01
Primary completion
2012-12-01
Completion
2012-12-01
First posted
2006-07-18
Last updated
2013-06-18

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00353613. Inclusion in this directory is not an endorsement.