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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03687216
Other study ID # HGT-EN
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date September 2019
Est. completion date December 2020

Study information

Verified date March 2019
Source West China Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A single-center randomized controlled study comparing endoscopic or interventional therapy guided by the hepatic venous pressure gradient (HVPG) , to standard endosopic variceal ligation plus nonselective beta-blocker therapy (NSBB) in patients with esophageal varices due to liver cirrhosis with a history of esophageal variceal hemorrhage.Primary study outcome of the study is variceal rebleeding episodes occurring within the first years after interventions. Second study outcomes of the study are hepatic encephalopathy occurrence, mortality occurrence, liver transplantation or other cirrhosis-related complications.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 160
Est. completion date December 2020
Est. primary completion date September 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- Liver cirrhosis diagnosed by clinical examination, imaging or biopsy;

- A previous history of variceal hemorrhage;

- Written informed consent.

Exclusion Criteria:

- Previous history of secondary prophylactic treatment;

- Contraindications to treatment of endoscopy, surgery and TIPS

- Severe cardiac, pulmonary or renal dysfunction;

- Lactating or pregnant;

- Malignancies;

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
HVPG-guided therapy
The baseline HVPG measurement is performed. According to the result, patients with an HVPG over 20 mmHg will be receive transjugular intrahepatic portocaval shunt (TIPS) . Patients with an HVPG below 20 mmHg will be treated by endoscopic variceal ligation (EVL) plus nonselective beta blocker (NSBB) propranolol until treatment fails.
Routing Therapy
Without HVPG measurement, patients receive endoscopic variceal ligation (EVL) plus nonselective beta blocker (NSBB) propranolol.

Locations

Country Name City State
China West China Hospital Chengdu Sichuan

Sponsors (1)

Lead Sponsor Collaborator
West China Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Variceal rebleeding rate The incidence of clinically significant gastrointestinal variceal bleeding One year of follow-up
Secondary Hepatic encephalopathy: The incidence of hepatic encephalopathy The incidence of hepatic encephalopathy One year of follow-up
Secondary Ascites: The incidence of ascites detected by ultrasound The incidence of ascites detected by ultrasound One year of follow-up
Secondary Cirrhotic complications portal vein thrombosis, liver dysfunction, hepatorenal syndrome et al. One year of follow-up
Secondary Liver transplant-free survivial Time from the procedure to the date of lost-to-follow-up or death or liver transplant One year of follow-up
See also
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Completed NCT04125875 - Gastric Slow Wave and Autonomic Nervous Function in Cirrhotic Patients With Esophageal Varices After Ligation-A Clinical Research
Completed NCT03943784 - Endoscopic Variceal Ligation in Children
Withdrawn NCT03373123 - Radiomics-based Surrogate of Endoscopy (rEndosc) (CHESS1703) N/A