Skip to content

Albumin in Acute Variceal Bleeding

Albumin in Acute Variceal Bleeding: A Randomized Controlled Trial: ALB-AVB Trial

Status
Not yet recruiting
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07395141
Acronym
ALB-AVB
Enrollment
60
Registered
2026-02-09
Start date
2026-03-01
Completion date
2026-05-31
Last updated
2026-02-09

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

Conditions

Acute Variceal Bleeding, Cirrhosis

Keywords

albumin, acute variceal bleed, cirrhosis, Albumin in acute variceal bleeding

Brief summary

The objective of this randomized control clinical trial is to learn the role of albumin in patients with acute variceal bleed. The trial will include all adult patients with acute variceal bleeding and cirrhosis presenting to Medical Gastroenterology department at KGMU, Lucknow, U.P. India, will include patients with age between 18-70 years and all gender. The primary endpoint will be re-bleeding during hospitalization and at 6 weeks. Participants will be randomized in two groups, the intervention group will receive albumin for 3 days along with standard treatment and comparison group will receive on standard treatment.

Detailed description

Albumin in acute variceal bleeding: A randomized controlled trial: ALB-AVB Trial Introduction: Albumin has been found to reduce mortality in patients with acute variceal bleeding in retrospective trials. However, there is no prospective data on this issue. We aim to conduct a randomized controlled trial on the role of albumin in patients with acute variceal bleeding. Review of the literature Acute variceal bleeding is an important decompensating event in patients with cirrhosis. It is associated with 20-30% mortality in six weeks. Standard therapy with splanchnic vasoconstrictors and endoscopic band ligation is the mainstay of treatment. Previous studies have shown that albumin may decrease the mortality and re-bleeding rate in patients with AVB, however, there is no prospective data on this. Apart from its oncotic properties albumin has different pleiotropic effects in patients with cirrhosis. It is an anti-oxidant and also binds to cytokines. Its anti-inflammatory property is responsible for reducing portal pressure and the risk of rebleeding. Currently, albumin is used in patients with acute kidney injury, spontaneous bacterial peritonitis and during large-volume paracentesis. There is also a theoretical risk of an increase in portal pressure in patients receiving albumin. The role of albumin in AVB is largely unknown. The current recommendation does not support its use in AVB however there is no strong evidence against it too. Currently, albumin has been shown to decrease mortality and decompensation in patients with cirrhosis. Large retrospective data from China have shown that albumin infusion is associated with reduced risk of rebleeding and mortality. In that study IV albumin of 40 grams/ day was associated with reduced mortality in patients with CTP-C cirrhosis. A perfectly designed RCT is warranted to explore the role of albumin in ABV. Aim of the study: To explore the role of albumin in patients with AVB. Study Methodology: It will be a randomised controlled trial conducted in the department of gastroenterology, KGMU Study Centre: Department of Gastroenterology, King George Medical University Lucknow Duration of the study: 6 months after the ethical approval Sample Size Calculation: Primary Outcome: The primary endpoint is re-bleeding during hospitalization and at 6 weeks. Standard Statistical Assumptions: Expected re-bleeding rate in the control group (no albumin): 30% Expected reduction with intervention (albumin): 15% Significance level (α): 0.05 Power (1-β): 0.8 Formula for Binary Outcomes (Re-bleeding or No Re-bleeding): n=(〖〖(Z〗\_(∝/2)+Z\_β)〗\^2×\[p\_1 (1-p\_1 )+p\_2 (1-p\_2 )\])/(p\_1-p\_2 )\^2 Where: p1=0.30 (control event rate) p2=0.15 (intervention event rate) Zα/2=1.96 (for 95% confidence) Zβ=0.84 (for 80% power) Adding an attrition of minimum to 5% (0.05), the sample size for study obtained was that of 126 patients that is 63 patients in each arm. But for feasibility purposes it was rounded off to achieve a final sample size of 60 patients randomly allocated in each arm.

Interventions

DRUGAlbumin

All the participants with acute variceal bleed will be given albumin along with standard treatment

Sponsors

King George's Medical University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Intervention model description

Parallel group randomized controlled trial

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* All adult patients with acute variceal bleeding and cirrhosis presenting to Medical Gastroenterology department at KGMU, Lucknow, U.P. India.

Exclusion criteria

1. Age \< 18 years and \> 70 years 2. Patients with portal vein thrombosis 3. Hepatocellular carcinoma 4. Non-cirrhotic portal fibrosis 5. Extrahepatic portal vein thrombosis 6. Patients who received albumin in the last one month 7. Patients who require fresh frozen plasma 8. Patients with heart failure 9. Patients with chronic kidney disease 10. Volume overload state

Design outcomes

Primary

MeasureTime frameDescription
Re-bleeding rateSix weeks (Baveno VII Consensus)All patients will receive vasoconstrictors after the initial hemodynamic resuscitation. Patients will receive terlipressin/ octreotide along with standard medical and endoscopic therapy. The intervention planned is administration of Albumin 40 mg/day and in comparison group only standard treatment will be given Re-bleeding rate in hospital and at six weeks will be measured. Time phrame is six weeks from the event.
In hospital mortalityFrom enrollment to death or discharge, other outcome is measured in six weeksAll patients will receive vasoconstrictors after the initial hemodynamic resuscitation. Patients will receive terlipressin/ octreotide along with standard medical and endoscopic therapy. The intervention planned is administration of Albumin 40 mg per day and in comparison group only standard treatment will be given In hospital mortality in both groups will be measured Time frame is six weeks

Secondary

MeasureTime frameDescription
MortalityFrom enrollment to 42 days (Baveno VII Consensus)All patients will receive vasoconstrictors after the initial hemodynamic resuscitation. Patients will receive terlipressin/ octreotide along with standard medical and endoscopic therapy. The intervention planned is administration of Albumin 40 mg/day and in comparison group only standard treatment will be given Mortality rate at 42 days will be measured
Need for rescue therapyFrom hospitalization to need for rescue therapy within 42 days of enrollment (Baveno VII Consensus)All patients will receive vasoconstrictors after the initial hemodynamic resuscitation. Patients will receive terlipressin/ octreotide along with standard medical and endoscopic therapy. The intervention planned is administration of Albumin 40 mg/day and in comparison group only standard treatment will be given Need for rescue therapy rate will be measured during hospitalization

Countries

India

Contacts

CONTACTDr Sumit Rungta, DM- Medical Gastroenterology
drsumitrungta79@gmail.com+919935537944
CONTACTDr Sayan Malakar, DM- Medical Gastroenterology
oneandonludrsayan@gmail.com+919007057890

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 10, 2026