- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02795091
Comparision of Different Methods of Enviromennt Disinfection
June 10, 2016 updated by: Chun Pan
Multidrug resistance bacteria infection is common in ICU.
Infection incidence is associated with age, organ dysfunction, invasive treatment and enviroment cleaning.
According to hospital hygienic standard for disinfection, total numbers of colony of air and the object surface in ICU must be ≤4CFU/cm2(5min)and≤10CFU/cm2.
in this study, the two different methods will be used to evaluate the disinfection effects in ICU enviroments.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Anticipated)
480
Phase
- Phase 2
- Phase 3
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 80 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
no patients recruitment
Exclusion Criteria:
no patients recruitment
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Screening
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: Manual clean
clean the rag and floor towel manually
|
manual clean the rag and floor towel
|
|
Other: machine clean
clean the rag and floor towel by machine
|
machine clean the rag and floor towel
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
incidence of infection
Time Frame: up to one month
|
up to one month
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
dose of antibiotics
Time Frame: up to one month
|
up to one month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
December 1, 2016
Primary Completion (Anticipated)
June 1, 2017
Study Completion (Anticipated)
June 1, 2017
Study Registration Dates
First Submitted
June 5, 2016
First Submitted That Met QC Criteria
June 5, 2016
First Posted (Estimate)
June 9, 2016
Study Record Updates
Last Update Posted (Estimate)
June 13, 2016
Last Update Submitted That Met QC Criteria
June 10, 2016
Last Verified
June 1, 2016
More Information
Terms related to this study
Other Study ID Numbers
- enviromennt disinfection
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Undecided
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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