- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03616366
The Mechanism and Prognosis of Pulmonary Circulation Dysfunction
July 27, 2018 updated by: Jianguo He, Chinese Academy of Medical Sciences, Fuwai Hospital
The Mechanism and Prognosis of Pulmonary Circulation Dysfunction in Pulmonary Injury and Recovery
Venous thromboembolism (VTE) is a condition which influenced by both environmental and genetic factors.
This study is going to explore new significant Single nucleotide polymorphisms (SNPs) associated with VTE by Genome-Wide Association Studies (GWAS) and bioinformatics analysis.
Transcriptomics and cytokine antibody array are also used to find new biomarkers of VTE's early diagnosis, severity and prognosis.
Study Overview
Status
Unknown
Conditions
Study Type
Observational
Enrollment (Anticipated)
1000
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
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Beijing, Beijing, China, 100037
- Recruiting
- Cardiovascular Institute and Fu Wai Hospital
-
Contact:
- Jianguo He, MD
- Phone Number: 86 01088398060
- Email: hejianguofw@163.com
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Principal Investigator:
- Jianguo He, MD
-
-
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
14 years and older (Child, Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Acute VTE patients and healthy controls
Description
Inclusion Criteria:
- Chinese Han population older than 14 years old
- Acute VTE patients diagnosed in 1 month
- With informed consent
Exclusion Criteria:
- Patients with psychosis
- Patients with contraindications for computed tomographic pulmonary angiography (CTPA)
- Chronic VTE
- Recurrence of chronic VTE
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 |
|---|---|---|
|
All cause death
Time Frame: 6 months
|
death
|
6 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Venous thromboembolism (VTE) recurrence
Time Frame: 6months
|
VTE recurrence detected by echocardiography or CTPA scan
|
6months
|
|
chronic thromboembolism pulmonary hypertension(CTEPH)
Time Frame: 6 months
|
newly developed CTEPH detected by pulmonary angiography
|
6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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 (Anticipated)
August 10, 2018
Primary Completion (Anticipated)
December 31, 2020
Study Completion (Anticipated)
December 31, 2020
Study Registration Dates
First Submitted
January 4, 2018
First Submitted That Met QC Criteria
July 27, 2018
First Posted (Actual)
August 6, 2018
Study Record Updates
Last Update Posted (Actual)
August 6, 2018
Last Update Submitted That Met QC Criteria
July 27, 2018
Last Verified
July 1, 2018
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2017-I2M-1-009
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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