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1 day vs 3 days of terlipressin therapy in cirrhosis patients with variceal bleeding

Not Applicable
Completed
Conditions
Health Condition 1: - Health Condition 2: K74- Fibrosis and cirrhosis of liver
Registration Number
CTRI/2019/10/021771
Lead Sponsor
Dr Shalimar
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1. (compensated or decompensated) with acute variceal bleeding

2.Willing to participate in the study

Exclusion Criteria

1.Variceal bleeding secondary to causes other than cirrhosis. eg, extrahepatic venous obstruction, hepatic venous outflow tract obstruction

2.Patients with malignancy/disseminated intravascular coagulation (DIC)/known coagulopathic disorder (hemophilia) apart from cirrhosis.

3.History of intake of platelets inhibitors (e.g., aspirin, clopidogrel) and drugs affecting coagulation cascade (e.g., vitamin K antagonists) within the past 7 days

4.Pregnant women

5.Patients with chronic renal failure

6.Patients with shock or requiring mechanical ventilation

7.Sepsis

8.Acute on chronic liver failure

9.Hepatorenal syndrome

10.Hepatic encephalopathy

11.Contraindication to endoscopy

12.Not willing to provide consent

13.Active angina, Recent Myocardial infarction or dynamic EKG changes

14.Failure to control variceal bleed on initial endoscopy

15.Isolated gastric variceal bleeding

16.Spontaneous bacterial peritonitis at presentation

17.Hepatocellular carcinoma or other liver metastatic malignancy

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1.Control of variceal bleeding at 24 hours and 5-days.Timepoint: 1.Control of variceal bleeding at 24 hours and 5-days.
Secondary Outcome Measures
NameTimeMethod
1.Rebleeding and mortality at 6 weeks. <br/ ><br>2.Difference in hepatic venous pressure gradient between the 2-groups at 1, 2 and 3 days post endoscopic variceal band ligationTimepoint: 6 weeks
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