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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02468479
Other study ID # CAWV-LC
Secondary ID
Status Completed
Phase N/A
First received June 4, 2015
Last updated April 18, 2017
Start date June 2015
Est. completion date December 2016

Study information

Verified date April 2017
Source General Hospital of Shenyang Military Region
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Chest/abdominal wall varices and spider nevi are two common presenting signs of liver cirrhosis. Their prognostic values remain unclear.


Recruitment information / eligibility

Status Completed
Enrollment 200
Est. completion date December 2016
Est. primary completion date December 2016
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

1. Liver cirrhosis.

2. Consecutive admission.

3. Permitted to physical examinations.

4. Informed consents.

Exclusion Criteria:

1. Non-cirrhotic portal hypertension.

2. Malignancy.

3. Uncontrolled infection.

4. Severe chronic diseases.

5. Poor patient compliance.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
No relevant intervention.
No relevant intervention.

Locations

Country Name City State
China Department of Gastroenterology, General Hospital of Shenyang Military Area Shenyang Liaoning

Sponsors (1)

Lead Sponsor Collaborator
General Hospital of Shenyang Military Region

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Prevalence and type of chest/abdominal wall varices and spider nevi Baseline data 1.5 years
Primary Association between etiology of liver cirrhosis and type of chest/abdominal wall varices and spider nevi Baseline data 1.5 years
Primary Association between degree of liver function and type of chest/abdominal wall varices and spider nevi Baseline data 1.5 years
Primary Effect of chest/abdominal wall varices and spider nevi on survival Follow-up data 2.5 years or more
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