Status:

UNKNOWN

Effects of Somatostatin on Post-endoscopic Portal Hemodynamic in Cirrhotic Patients With Esophageal Gastric Varices

Lead Sponsor:

Yunsheng Yang

Conditions:

Esophageal Varices Secondary to Cirrhosis of Liver

Eligibility:

All Genders

18-75 years

Phase:

NA

Brief Summary

The main complications of cirrhosis are ascites, esophageal varices and hepatic encephalopathy. About 30% to 70% patients with cirrhosis occur esophageal varices, and the most common complication is a...

Detailed Description

126 patients will be enrolled in the study, 63 subjects will be randomized into the group A and the other will be into the group B. Group A: endoscopic therapy and somatostatin treatment. Group B: en...

Eligibility Criteria

Inclusion

  • Cirrhosis with esophageal gastric varices needed endoscopic therapy
  • Age 18-75 years
  • Informed written consent

Exclusion

  • Use of vasoactive drugs 24 hours before endoscopic treatment
  • Use of B-blocker within 1 week
  • Previous surgical or endoscopic treatment for esophageal gastric varices
  • Hepatic encephalopathy,comatose status and any other disease which could not accept endoscopic therapy
  • Gastro-renal vein shunt
  • Severe hepatic hydrothorax
  • Hepatocellular carcinoma with portal vein thrombosis
  • Severe coagulation disorders
  • Severe active bacteria infection
  • Severe cardiovascular disease, including a history of acute myocardial infarction,heart block, heart failure
  • Severe renal function insufficiency (Calculated Creatinine Clearance Rate (Ccr) \<30ml/min)
  • Severe co-morbidity that would affect short-term prognosis
  • Pregnancy or lactation
  • Allergy to any ingredient of trial medication
  • Medical or psychological condition that would not permit the patient to complete the study or sign the informed consent

Key Trial Info

Start Date :

July 1 2011

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

December 1 2012

Estimated Enrollment :

126 Patients enrolled

Trial Details

Trial ID

NCT01426087

Start Date

July 1 2011

End Date

December 1 2012

Last Update

September 2 2011

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Site

Beijing, China, 010