Liver Cirrhosis
Conditions
Brief summary
Acute variceal bleeding (AVB) in cirrhosis occurs as a result of portal hypertension and carries a 6-week mortality rate of approximately 10-20%. Standard management includes a restrictive transfusion approach, vasoactive therapy, prophylactic antibiotics, and endoscopic band ligation. Despite this, early rebleeding within the first 5 days still occurs in about 10-20% of patients, and individuals at particularly high risk may benefit from pre-emptive TIPS. However, its real-world use remains limited; one study reported that only 6.7% of eligible patients actually underwent pre-emptive TIPS, primarily due to logistical challenges and limited interventional radiology availability for early, non-emergent TIPS procedures. Midodrine, an oral and fast-acting selective α1-adrenergic agonist, has been shown to enhance the effectiveness of nonselective beta-blockers like propranolol by allowing higher tolerated doses and achieving greater reductions in portal pressure (HVPG), thereby reducing the risk of initial variceal bleeding. However, no studies have evaluated the combination of midodrine with carvedilol-currently a preferred agent-versus carvedilol alone in patients at high risk of rebleeding. To address this gap, we propose a study comparing carvedilol plus midodrine with carvedilol alone for preventing early rebleeding in cirrhotic patients. Individuals with cirrhosis (Child-Pugh 8-13) presenting with hematemesis will be enrolled, stabilized according to APASL guidelines, and after 48 hours randomized to either combined midodrine-carvedilol therapy or carvedilol alone. Participants will be followed for 6 weeks to assess the incidence of early rebleeding.
Interventions
Carvedilol will be up-titrated by 3.125 mg daily to a maximum of 6.25 mg twice daily
Midodrine will be increased by 5 mg daily to a maximum of 15 mg three times daily (45 mg/day).
Sponsors
Study design
Eligibility
Inclusion criteria
1. Consecutive patients of cirrhosis with high-risk acute variceal bleed (Child-Pugh class B \> 7 with active bleeding at initial endoscopy or Child-Pugh class C \< 14 points).
Exclusion criteria
1. Age less than 18 years or \> 75 years. 2. HR \< 60/ min and BP \< 100/60 mm Hg 3. Child-Pugh's score \<8 and \>13. 4. MELD score \>30 and serum lactate \>12mmol/L. 5. Refractory variceal bleed. 6. Preemptive TIPS or previous Porto-systemic shunt or TIPS. 7. Non-selective Beta blocker/carvedilol / midodrine treatment in last 5 days. 8. Acute kidney injury - HRS. 9. Uncontrolled Hypertension (BP \> 140/90 mmHg), heart block, congestive heart failure. 10. Contraindication to NSBB (HR\<60/min, BP\<90/60mmHg, bronchial asthma). 11. Hepatocellular carcinoma (outside Milan criteria), extrahepatic malignancy. 12. Pregnant women. 13. Bleeding from isolated gastric or ectopic varices.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Proportion of patients with early variceal rebleed in 6 weeks in both the groups. | 6 weeks |
Secondary
| Measure | Time frame |
|---|---|
| Liver transplant free survival at 6 weeks. | 6 weeks |
| Blood products Transfusion at 6 weeks. | 6 weeks |
| Need of rescue therapy at 6 weeks (Danis Ella stent / Sengstaken tube/ rescue TIPS). | 6 weeks |
| Change in HVPG at 4 weeks. | 4 weeks |
| New decompensation and further decompensation at 6 weeks | 6 weeks |
| ICU stay and hospital stay duration. | 6 weeks |
| Change in MELD score | 6 weeks |
| Mean carvedilol dose in both groups at 6 weeks. | 6 weeks |
| Adverse events at 6 weeks | 6 weeks |
Countries
India