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Carvedilol and Midodrine Versus Carvedilol Alone in Preventing Early Rebleed in Patients With Cirrhosis.

Carvedilol and Midodrine Versus Carvedilol Alone in Preventing Early Rebleed in Patients With Cirrhosis: A Randomized Controlled Trial.

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07465471
Enrollment
210
Registered
2026-03-12
Start date
2026-03-01
Completion date
2027-09-30
Last updated
2026-03-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Liver Cirrhosis

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

DRUGCarvedilol

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

Institute of Liver and Biliary Sciences, India
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

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

MeasureTime frame
Proportion of patients with early variceal rebleed in 6 weeks in both the groups.6 weeks

Secondary

MeasureTime 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 weeks6 weeks
ICU stay and hospital stay duration.6 weeks
Change in MELD score6 weeks
Mean carvedilol dose in both groups at 6 weeks.6 weeks
Adverse events at 6 weeks6 weeks

Countries

India

Contacts

CONTACTDr Meenakshi S Mann, DNB
meenakshimann22@gmail.com01146300000
CONTACTDr Chitranshu Vashishtha, DM
chitranshuv@gmail.com01146300000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 13, 2026