- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05166759
Incidence and Clinical Characteristics of Pulmonary Hypertension Secondary to ARDS in the Highland
December 21, 2021 updated by: Chun Pan, Southeast University, China
Incidence and Clinical Characteristics of Pulmonary Hypertension Secondary to ARDS
The study is conducted in the affiliated hospital of Qinghai University .Patients in the department of Critical Care Medicine and Emergency Intensive Care Unit will be eligible for inclusion if they meet the Berlin criteria.Two researchers assess pulmonary artery pressure and right heart function of patients who are enrolled.
Study Overview
Study Type
Observational
Enrollment (Anticipated)
100
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Chun Pan, MD
- Phone Number: 13814009925
- Email: panchun1982@gmail.com
Study Contact Backup
- Name: Peng Zhu
- Phone Number: 18625195060
- Email: sqzhupeng@163.com
Study Locations
-
-
Qinghai
-
Xining, Qinghai, China
- Recruiting
- Affiliated Hospital of Qinghai University
-
Contact:
- Chun Pan, MD
- Phone Number: 13814009925
- Email: panchun1982@gmail.com
-
-
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
Sampling Method
Non-Probability Sample
Study Population
The study is conducted in the affiliated hospital of Qinghai University .Patients in the department of Critical Care Medicine and Emergency Intensive Care Unit will be eligible for inclusion if they meet the Berlin criteria.Two researchers assess pulmonary artery pressure and right heart function of patients who are enrolled.
Description
Inclusion Criteria:
Inclusion Criteria:
18 to 80 years of age Meet the diagnostic criteria Receive invasive mechanical ventilation within 48 hours
-
Exclusion Criteria:
Patients with those disease will be excluded : chronic obstructive pulmonary disease Pulmonary embolism Chronic heart failure Idiopathic pulmonary fibrosis Pulmonary hypertension Pregnant women will be excluded too.
-
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Incidence of Pulmonary Hypertension Secondary to ARDS in the Highland
Time Frame: 20/11/2021-20/12/2022
|
20/11/2021-20/12/2022
|
|
ICU mortality ICU mortality
Time Frame: 20/11/2021-20/12/2022
|
Mortality during treatment in ICU
|
20/11/2021-20/12/2022
|
28-days mortality rate
Time Frame: 20/11/2021-20/12/2022
|
Mortality at 28 days of hospitalization
|
20/11/2021-20/12/2022
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Ventilator time
Time Frame: 20/11/2021-20/12/2022
|
Ventilator time in ICU
|
20/11/2021-20/12/2022
|
Hospital length of stay
Time Frame: 20/11/2021-20/12/2022
|
Total length of stay in hospital
|
20/11/2021-20/12/2022
|
Other Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Right cardiac functionof Pulmonary Hypertension Secondary to ARDS in the Highland
Time Frame: 20/11/2021-20/12/2022
|
20/11/2021-20/12/2022
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Chun Pan, MD, Qinghai University
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)
November 25, 2021
Primary Completion (Anticipated)
March 1, 2022
Study Completion (Anticipated)
December 1, 2022
Study Registration Dates
First Submitted
December 20, 2021
First Submitted That Met QC Criteria
December 21, 2021
First Posted (Actual)
December 22, 2021
Study Record Updates
Last Update Posted (Actual)
December 22, 2021
Last Update Submitted That Met QC Criteria
December 21, 2021
Last Verified
November 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ARDS in the highland
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
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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