- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02460939
The Study on the Pulmonary Vessel Disease and Its Changes in Metabolism of Small Molecules
June 2, 2015 updated by: Yingmin Ma, Beijing Chao Yang Hospital
The Study on the Pulmonary Vessel Disease and Its Its Changes in Metabolism of Small Molecules
The purpose of this study is to investigate the changes of the pulmonary vessel disease and its metabolism of small molecules.
Study Overview
Status
Unknown
Conditions
Detailed Description
The patient with acute respiratory distress syndrome and sepsis come to hospital ,the investigators will blood them to study the changes in metabolism of small molecules.
Study Type
Observational
Enrollment (Anticipated)
18
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, 100020
- Recruiting
- Liu Sijie
-
Contact:
- sijie liu, bachelor
- Phone Number: 15210511726
- Email: lsijie1990@163.com
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Principal Investigator:
- yingmin ma, dooctor
-
-
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 85 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Patients with ARDS and sepsis or only sepsis aged between 45 and 85
Description
Inclusion Criteria:the aged between 18 and 85;Patients with ARDS and sepsis;Patients with only sepsis;normal
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Exclusion Criteria:Age <18 or >85, pregnancy, diabetes mellitus, cardiac pulmonary edema, can lead to other conditions of ARDS: severe trauma, a large number of blood transfusions, severe acute pancreatitis, etc., end-stage tumor.
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
- Observational Models: Case-Only
- Time Perspectives: Retrospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
The changes of patients'metabolism of small molecules
Time Frame: about 10 days
|
about 10 days
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: yingmin ma, Vice President of the Beijing chaoyang 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
August 1, 2014
Primary Completion (Anticipated)
January 1, 2016
Study Completion (Anticipated)
August 1, 2016
Study Registration Dates
First Submitted
June 1, 2015
First Submitted That Met QC Criteria
June 2, 2015
First Posted (Estimate)
June 3, 2015
Study Record Updates
Last Update Posted (Estimate)
June 3, 2015
Last Update Submitted That Met QC Criteria
June 2, 2015
Last Verified
June 1, 2015
More Information
Terms related to this study
Other Study ID Numbers
- 12704102
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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