Liver Cirrhosis Clinical Trial
Official title:
Thoracoscopic Mesh Repair of Diaphragmatic Defects for Hepatic Hydrothorax: 10 Years' Experience From a Single Large-volume Center
Verified date | July 2015 |
Source | National Taiwan University Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | Taiwan: Department of Health |
Study type | Interventional |
The management of refractory hepatic hydrothorax is challenging and usually unsuccessful. The study will discuss the perioperative treatment, effectiveness, and morphology of diaphragmatic defects of hepatic hydrothorax in thoracoscopic mesh repair. Risk factors associated with increased three-month mortality in these critically ill patients will be studied.
Status | Completed |
Enrollment | 63 |
Est. completion date | June 2015 |
Est. primary completion date | December 2014 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: - patients with refractory hepatic hydrothorax (> 3 times thoracentesis and failure to maximal doses of diuretics) Exclusion Criteria: - Patients with systemic bacteremia, positive culture of bacteria of pleural effusion or ascites were excluded from the study because of potential mesh contamination. |
Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
National Taiwan University Hospital |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | one-month mortality | one-month mortality after thoracoscopic mesh repair | one month | Yes |
Primary | three-month mortality | three-month mortality after thoracoscopic mesh repair | three month | Yes |
Secondary | recurrence of hepatic hydrothorax | recurrence of hepatic hydrothorax after thoracoscopic mesh repair | 20.5 months | Yes |
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