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NCT Number: NCT07465471

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

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.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Institute of Liver and Biliary Sciences

New Delhi, National Capital Territory of Delhi, 110070, India

Location contact

Dr Meenakshi Mann, DNB

CONTACT

[email protected]

01146300000

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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

  • Age less than 18 years or > 75 years.
  • HR < 60/ min and BP < 100/60 mm Hg
  • Child-Pugh's score <8 and >13.
  • MELD score >30 and serum lactate >12mmol/L.
  • Refractory variceal bleed.
  • Preemptive TIPS or previous Porto-systemic shunt or TIPS.
  • Non-selective Beta blocker/carvedilol / midodrine treatment in last 5 days.
  • Acute kidney injury - HRS.
  • Uncontrolled Hypertension (BP > 140/90 mmHg), heart block, congestive heart failure.
  • Contraindication to NSBB (HR<60/min, BP<90/60mmHg, bronchial asthma).
  • Hepatocellular carcinoma (outside Milan criteria), extrahepatic malignancy.
  • Pregnant women.
  • Bleeding from isolated gastric or ectopic varices.

Treatment and study plan

Carvedilol

Drug

Carvedilol will be up-titrated by 3.125 mg daily to a maximum of 6.25 mg twice daily

Midodrine Oral Product

Drug

Midodrine will be increased by 5 mg daily to a maximum of 15 mg three times daily (45 mg/day).

Primary outcomes

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

    Time frame: 6 weeks

Secondary outcomes

  1. Liver transplant free survival at 6 weeks.

    Time frame: 6 weeks

  2. Blood products Transfusion at 6 weeks.

    Time frame: 6 weeks

  3. Need of rescue therapy at 6 weeks (Danis Ella stent / Sengstaken tube/ rescue TIPS).

    Time frame: 6 weeks

  4. Change in HVPG at 4 weeks.

    Time frame: 4 weeks

  5. New decompensation and further decompensation at 6 weeks

    Time frame: 6 weeks

  6. ICU stay and hospital stay duration.

    Time frame: 6 weeks

  7. Change in MELD score

    Time frame: 6 weeks

  8. Mean carvedilol dose in both groups at 6 weeks.

    Time frame: 6 weeks

  9. Adverse events at 6 weeks

    Time frame: 6 weeks

Study contacts

Contact information is provided by the study sponsor or research team.

Dr Chitranshu Vashishtha, DM

CONTACT

[email protected]

01146300000

Dr Meenakshi S Mann, DNB

CONTACT

[email protected]

01146300000

Sponsors and collaborators

Lead sponsor

Institute of Liver and Biliary Sciences, India

Other

Registry information

Official study title

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

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Mar 12, 2026
Registry last updated
Mar 12, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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