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Investigation of the Prevalence of Hepatopulmonary Syndrome in Cirrhosis Patients Caused by Hepatitis B in Western China

Investigation of the Prevalence of Hepatopulmonary Syndrome in Cirrhosis Patients Caused by Hepatitis B in Western China

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03435406
Enrollment
300
Registered
2018-02-19
Start date
2017-07-27
Completion date
2018-04-01
Last updated
2018-02-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hepatopulmonary Syndrome

Keywords

Hepatitis B, Chronic, Cirrhosis, Hepatopulmonary Syndrome

Brief summary

to investigate the prevalence of hepatopulmonary syndrome in cirrhosis patients caused by Hepatitis B in western China

Detailed description

Hepatopulmonary syndrome (HPS) occurs in approximately 4%-29% of cirrhotic patients and influences mortality. China has 100 million Hepatitis B virus (HBV) carriers and Chronic HBV infection is well-recognized risk factor for cirrhosis.But little is known about the prevalence of HPS in cirrhosis patients caused by HBV in western China. The aim of this study was to investigate the HPS incidence, and the signs, symptoms, arterial blood gas, and BMP9 in the serum of the patients.

Interventions

None listed

Sponsors

Southwest Hospital, China
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. Age: 18-80 years old; 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

1. Severe heart, lung, kidney disease coexisted; 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.

Design outcomes

Primary

MeasureTime frameDescription
oxygen saturationDuring the operationoxygen saturation was examined by pulse oximetry
spider angiomaDuring the operationspider angioma was examined by inspection
liver palmsDuring the operationliver palms was examined by inspection
transthoracic contrast enhanced echocardiography (CEE)During the operationthrough the ultrasound to evaluate the imagine of cardiac cavity after intravenous injection of agitated saline
arterial blood gasDuring the operationarterial blood gas analysis was performed through the radial artery.
medical historyDuring the operationThe medical history was collected through consultation.
acropachyDuring the operationacropachy was examined by inspection

Secondary

MeasureTime frameDescription
micro ribonucleic acid 144 (miR144), micro ribonucleic acid 200 (miR200) in the patients with and without HPS4 to 6 months after the study completionthe content and expression of BMP9 were determined by polymerase chain reaction (PCR)
the content of bone morphogenetic protein (BMP9) in the patients with and without HPS4 to 6 months after the study completionthe content and expression of BMP9 were determined by immunohistochemistry.

Countries

China

Contacts

Primary ContactYi Bin, PhD
tang123a123123@163.com0086-02368754197
Backup Contacttang xi, md
12923699@qq.com0086-18623198332

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026