Investigation of the Prevalence of Hepatopulmonary Syndrome in Cirrhosis Patients Caused by Hepatitis B in Western China
NCT ID: NCT03435406
Last Updated: 2018-02-19
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
300 participants
OBSERVATIONAL
2017-07-27
2018-04-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
CROSS_SECTIONAL
Study Groups
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cirrhosis with HPS
Diagnosed as HPS
No interventions assigned to this group
cirrhosis without HPS
Not Diagnosed as HPS
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
2. American association of anesthesiologists(ASA) score: I-III;
3. Ability to comply with research programmes;
4. Voluntary participation in the study;
5. Has the history of HBV infection;
6. No primary cardiopulmonary disease (heart disease, emphysema, pneumonia, asthma, etc.)
Exclusion Criteria
2. American association of anesthesiologists(ASA) score≥IV; forced expiratory volume at one second (FEV1) or forced vital capacity (FVC) \<70%, or FEV1 / FVC \<0.70;
3. Mental state could not cooperate
4. Absence of written informed consent.
18 Years
80 Years
ALL
No
Sponsors
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Southwest Hospital, China
OTHER
Responsible Party
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Lu KZ
Professor of Institute of Anesthesiology, Southwest Hospital, Third Military Medical University Affiliation: Southwest Hospital, China
Principal Investigators
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Lu K Zhi, PhD
Role: STUDY_DIRECTOR
Department of Anesthesiology, Southwest Hospital Third Military Medical University
Locations
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Department of Anesthesiology, Southwest Hospital Third Military Medical University
Chongqing, Chongqing Municipality, China
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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CEE-HBV
Identifier Type: -
Identifier Source: org_study_id
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