- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04954300
Investigation on the Dynamic Changes in Air Microbiome in Intensive Care Unit
May 31, 2023 updated by: Peking University Third Hospital
The microbiome of ICU, especially the air microbiome of ICU is not clear.
The relationship between the microbiome of ICU and the hospital- acquired infection needs to be clarified.
In this study, we try to outline the dynamic changes of microbiome in ICU and give some advice on the prevention of HAI.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
500
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Beijing
-
Beijing, Beijing, China, 100191
- Peking University Third Hospital
-
-
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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
No patients were enrolled in this study.
Description
Inclusion criteria: no patients were enrolled in this study.
Exclusion criteria: no patients were enrolled in this study.
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
open
open: open ICU
|
No intervention
|
|
negative
negative: negative-pressure laminar flow ward
|
No intervention
|
|
positive
positive: laminar flow ward
|
No intervention
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Community of microbiome in ICU
Time Frame: 1 year and a half
|
the dynamic changes of metagenomic/16s sequencing data
|
1 year and a half
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Yuxin Leng, PhD, Peking University Third Hospital
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 (Actual)
February 1, 2021
Primary Completion (Actual)
August 1, 2022
Study Completion (Actual)
August 1, 2022
Study Registration Dates
First Submitted
June 29, 2021
First Submitted That Met QC Criteria
July 1, 2021
First Posted (Actual)
July 8, 2021
Study Record Updates
Last Update Posted (Estimated)
June 2, 2023
Last Update Submitted That Met QC Criteria
May 31, 2023
Last Verified
May 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- LM2021076
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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