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Completed Not applicable Interventional Accepts healthy volunteers Results available

Effect of Expanding (Gloving) Barrier Precautions for Reducing Clostridium Difficile Acquisition (and Infection) in VA

ClinicalTrials.gov ID: NCT04036058

Public ClinicalTrials.gov record NCT04036058. 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 Sep 6, 2026, 2:24 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

Effect of Expanding Barrier Precautions for Reducing Clostridium Difficile Acquisition in VA

Brief summary

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

Clostridium difficile (C. difficile) is a major pathogen causing serious healthcare-associated diarrheal illness in patients. Prevention of healthcare facility-onset C. difficile infection (CDI) is essential. Many CDI cases are caused by the transmission of the pathogen from patients who carry the bacteria, but do not have symptoms. However, there are limited data on how to prevent the transmission of C. difficile from patients who do not have symptoms. Universal gloving practices - the use of gloves by all healthcare workers for all patient contacts - may reduce CDI cases. In this study, the investigators will examine the effectiveness of universal gloving practices as compared to standard of care (use of gloving for contact only in patients with known CDI or other infections). The investigators will compare the effects of these practices on the transmission of C. difficile within participating hospital units to determine if universal gloving is an effective practice to prevent healthcare-associated CDI.

Study identification

NCT ID
NCT04036058
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Enrollment
780 participants

Conditions and interventions

Interventions

Other

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Accepts healthy volunteers

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

Study timeline

Start date
Mar 28, 2022
Primary completion
Dec 28, 2023
Completion
Sep 29, 2024
Last update posted
Jul 10, 2025

2022 – 2024

United States locations

U.S. sites
6
U.S. states
5
U.S. cities
6
Facility City State ZIP Site status
Washington DC VA Medical Center, Washington, DC Washington D.C. District of Columbia 20422-0001
Edward Hines Jr. VA Hospital, Hines, IL Hines Illinois 60141-3030
James J. Peters VA Medical Center, Bronx, NY The Bronx New York 10468-3904
VA Portland Health Care System, Portland, OR Portland Oregon 97207-2964
William S. Middleton Memorial Veterans Hospital, Madison, WI Madison Wisconsin 53705-2254
Clement J. Zablocki VA Medical Center, Milwaukee, WI Milwaukee Wisconsin 53295-0001

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 NCT04036058, 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 Jul 10, 2025 · Synced Sep 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04036058 live on ClinicalTrials.gov.

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