- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07372742
Clinical Characteristics and Epidemiology of Chronic Critically Ill Patients in China
This study aims to enroll chronic critically ill patients in ICU to investigate the epidemiology of chronic critically ill in China and identify risk factors of poor outcomes among those patients. The main question it aims to answer is:
What is the one year mortality of chronic critically ill patients in China? We conduct semi-structured telephone follow-ups to investigate the long-term outcomes of chronic critically ill patients.
Study Overview
Status
Conditions
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Locations
-
-
Sichuan
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Chengdu, Sichuan, China, 610041
- Recruiting
- West China Hospital of Sichuan University
-
Contact:
- Xuepeng Zhang, PhD
- Phone Number: 8615882249643
- Email: zhang_xuepeng@wchscu.cn
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Must meet: Age greater than 18 years old; Stay in ICU for 8 days or more.
Meet any of the following criteria:
Tracheotomy; Continuous mechanical ventilation for over 96 hours; Multiple organ failure; Sepsis or severe infection; Severe trauma; Severe brain injury;
Exclusion Criteria:
- Refusing to accept follow-up; Patients who have been lost to follow-up;
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
one year mortality
Time Frame: one year
|
one year mortality
|
one year
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 2026-01-12
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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