NCT02605499

Brief Summary

This study examines the impact of UV-C light disinfection as an adjunct to routine daily and discharge patient room cleaning on patient infection and colonization with hospital associated bacteria. Patient rooms are counted as enrolled since consent was waived and the number of participants is unknown. Total of 83 rooms.

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
83

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Dec 2015

Typical duration for not_applicable

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

November 11, 2015

Completed
5 days until next milestone

First Posted

Study publicly available on registry

November 16, 2015

Completed
15 days until next milestone

Study Start

First participant enrolled

December 1, 2015

Completed
2.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 1, 2018

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 1, 2018

Completed
Last Updated

September 19, 2018

Status Verified

September 1, 2018

Enrollment Period

2.2 years

First QC Date

November 11, 2015

Last Update Submit

September 17, 2018

Conditions

Outcome Measures

Primary Outcomes (2)

  • Acquisition of Vancomycin Resistant Enterococcus

    Rates of Vancomycin Resistant Enterococcus acquisition will be compared between intervention and control periods.

    2 years

  • Acquisition of a composite rate of healthcare-associated bacteria: Vancomycin Resistant Enterococcus, Methicillin Resistant Staphylococcus Aureus, hospital-onset bacteremias, Clostridium difficile, and central line associated bloodstream infections.

    Rates of Vancomycin Resistant Enterococcus, Methicillin Resistant Staphylococcus Aureus, hospital-onset bacteremias, multidrug resistant gram negative bacteria, Clostridium difficile, and central line associated bloodstream infections will be compared between intervention and control periods.

    2 years

Secondary Outcomes (13)

  • Acquisition of Vancomycin Resistant Enterococcus (clinical infection)

    2 years

  • Acquisition of Vancomycin Resistant Enterococcus (colonization)

    2 years

  • Acquisition of Clostridium difficile (infection)

    2 years

  • Acquisition of Clostridium difficile (colonization or infection)

    2 years

  • Acquisition of bacteremia

    2 years

  • +8 more secondary outcomes

Study Arms (2)

UV-C light disinfection

EXPERIMENTAL

During intervention UV-C light disinfection will be used in hospital patient rooms as an adjunct to routine daily and discharge cleaning.

Other: UV-C light disinfection

Control

NO INTERVENTION

During control period there will be standard discharge and daily room cleaning only, with no UV-C light disinfection.

Interventions

UV-C light disinfection will be used in hospital patient rooms as an adjunct to routine daily and discharge cleaning.

UV-C light disinfection

Eligibility Criteria

Age16 Years+
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Patient rooms in pre-selected hospital units within Johns Hopkins Hospital

You may not qualify if:

  • None, intervention is at level of the hospital unit, not the patient

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Related Publications (1)

  • Rock C, Hsu YJ, Curless MS, Carroll KC, Ross Howard T, Carson KA, Cummings S, Anderson M, Milstone AM, Maragakis LL. Ultraviolet-C Light Evaluation as Adjunct Disinfection to Remove Multidrug-Resistant Organisms. Clin Infect Dis. 2022 Aug 24;75(1):35-40. doi: 10.1093/cid/ciab896.

MeSH Terms

Conditions

Cross Infection

Condition Hierarchy (Ancestors)

InfectionsIatrogenic DiseaseDisease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Lisa Maragakis, MD, MPH

    Johns Hopkins University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
CROSSOVER
Model Details: Patient rooms are counted as enrolled since consent was waived and the number of participants is unknown. Total of 83 rooms.
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

November 11, 2015

First Posted

November 16, 2015

Study Start

December 1, 2015

Primary Completion

February 1, 2018

Study Completion

February 1, 2018

Last Updated

September 19, 2018

Record last verified: 2018-09