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RecruitingNCT07281846Updated Dec 15, 2025

TIPS With or Without BCAA

An interventional study of The BCAA Group (experimental group) takes oral branched-chain amino acid (BCAA) supplements for 3 months starting after TIPS. and The Placebo Group (control group) takes oral placebo for 3 months postoperatively-prepared by an independent third party, the placebo is identical to BCAA supplements in appearance, odor, and packagin in BCAA, Cirrhosis and Portal Hypertension Related to Cirrhosis, sponsored by Union Hospital, Tongji Medical College, Huazhong University of Science and Technology. Recruiting at 1 site in China. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2025-12-15.

Sponsored by Union Hospital, Tongji Medical College, Huazhong University of Science and Technology · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started Nov 2025; still recruiting 10 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
164
Allocation
Randomized
Ages
18 Years to 80 Years
Sex
All
01

Study summary

Cirrhosis is a major global cause of morbidity and mortality in chronic liver disease patients, accounting for 2.4% of global deaths in 2019. A 1990-2017 Global Burden of Disease study showed rising cirrhosis-related deaths, bringing heavy health and economic burdens. It often leads to portal hypertension and subsequent complications like ascites, gastroesophageal variceal bleeding (20% 6-week mortality), and hepatic encephalopathy (HE). Transjugular intrahepatic portosystemic shunt (TIPS) is an important treatment for variceal bleeding and refractory ascites per guidelines from EASL, AASLD, and the Chinese Medical Association.

Malnutrition affects 20% of compensated and over 50% of decompensated cirrhotic patients; sarcopenia (severe malnutrition) is linked to higher cirrhosis-related complications, impaired quality of life, survival, and poor prognosis in TIPS-treated patients. Thus, concurrent sarcopenia intervention during TIPS may improve outcomes.

Baveno VII, EASL, and AASLD guidelines recommend branched-chain amino acid (BCAA) and leucine-rich supplements for decompensated cirrhosis to ensure adequate nitrogen intake. RCT evidence shows BCAAs improve skeletal muscle index (SMI) in cirrhotic patients with sarcopenia and reduce HE risk, but evidence for TIPS-treated patients is lacking. This study aims to compare muscle mass changes and clinical prognosis between TIPS patients with sarcopenia, portal hypertension, and variceal bleeding who receive TIPS with or without BCAA supplements.

Read the detailed description

Cirrhosis is a major cause of morbidity and mortality among patients with chronic liver disease worldwide. In 2019, cirrhosis accounted for 2.4% of global deaths. A Global Burden of Disease study (1990-2017) showed that the number of deaths caused by cirrhosis has been on the rise year by year since 1990, imposing a severe health and economic burden on many countries and peoples around the world. Cirrhosis is usually accompanied by the development of portal hypertension, which further leads to complications such as ascites, gastroesophageal variceal bleeding, and hepatic encephalopathy (HE). Among these, the mortality rate of gastroesophageal variceal bleeding reaches as high as 20% within 6 weeks of onset. Currently, according to guidelines issued by the European Association for the Study of the Liver (EASL), the American Association for the Study of Liver Diseases (AASLD), and the Chinese Medical Association, transjugular intrahepatic portosystemic shunt (TIPS) has become an important treatment for variceal bleeding and refractory ascites.

Malnutrition is a common complication of cirrhosis, affecting 20% of patients with compensated cirrhosis and more than 50% of those with decompensated cirrhosis. Sarcopenia is generally regarded as severe malnutrition, and its occurrence is often associated with a higher risk of cirrhosis-related complications (such as hepatic encephalopathy, ascites, and infections), which seriously impairs patients' quality of life and survival. Several studies have shown that sarcopenia is associated with poor prognosis in cirrhotic patients undergoing TIPS treatment. Therefore, concurrent intervention for sarcopenia during TIPS treatment may improve prognosis and thus enhance patient survival.

The Baveno VII guidelines point out that malnutrition increases the risk of poor prognosis in patients with cirrhosis and acute variceal bleeding, and oral nutrition should be initiated as soon as possible. Both the EASL Clinical Practice Guidelines on Nutrition in Chronic Liver Disease and the AASLD Practice Guidance on Malnutrition, Frailty, and Sarcopenia in Patients with Cirrhosis recommend the use of branched-chain amino acid (BCAA) supplements and leucine-rich amino acid supplements in patients with decompensated cirrhosis to achieve adequate nitrogen intake. An RCT study demonstrated that BCAA supplements can improve the skeletal muscle index (SMI) in cirrhotic patients with sarcopenia. Additionally, evidence suggests that BCAA supplements can significantly reduce the risk of hepatic encephalopathy (HE).

Therefore, BCAA supplements may serve as a routine nutritional supplement for cirrhotic patients undergoing TIPS treatment, but relevant evidence is currently lacking. This study aims to compare changes in muscle mass and clinical prognosis between cirrhotic patients with portal hypertension and variceal bleeding complicated by sarcopenia who receive TIPS with or without BCAA supplements, so as to verify our hypothesis.

02

Conditions studied

  • BCAA
  • Cirrhosis
  • Portal Hypertension Related to Cirrhosis
  • Sarcopenia
  • Transjugular Intrahepatic Portosystemic Shunt

Keywords

  • Transjugular Intrahepatic Portosystemic Shunt
  • Sarcopenia
  • Portal Hypertension
  • Cirrhosis
  • BCAA
03

In context

Fibrosis

3,255 studies on the registry are indexed under Fibrosis; 465 are open to participants now.

This study's planned enrollment of 164 is above the median of 50 across 2,130 interventional studies indexed under Fibrosis.

Browse Fibrosis studies →

Lead sponsor

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology is the lead sponsor of 160 studies on the registry; 129 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Age between 18 and 80 years old;
  2. Diagnosed with cirrhosis complicated by sarcopenia;
  3. Patients admitted due to variceal bleeding or refractory ascites who meet the indications for transjugular intrahepatic portosystemic shunt (TIPS).

Exclusion criteria

Exclusion Criteria:

  1. Hepatocellular carcinoma and/or other malignant tumors;
  2. Severe cardiopulmonary insufficiency;
  3. Child-Pugh score > 13 points;
  4. Spontaneous recurrent hepatic encephalopathy (HE);
  5. Large spontaneous portosystemic shunt;
  6. Sepsis; spontaneous bacterial peritonitis (SBP);
  7. Allergy to any component of the study nutritional supplement;
  8. High-energy and high-protein diet or use of calcium supplements, vitamin D supplements, or protein/amino acid supplements within 3 months prior to the study.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
164 participants (estimated)

Study arms

  • Experimental
    BCAA Group

    The BCAA Group (experimental group) takes oral branched-chain amino acid (BCAA) supplements for 3 months starting after surgery.

    Dietary Supplement: The BCAA Group (experimental group) takes oral branched-chain amino acid (BCAA) supplements for 3 months starting after TIPS.

  • Placebo comparator
    Non-BCAA Group

    The Placebo Group (control group) takes oral placebo for 3 months postoperatively-prepared by an independent third party, the placebo is identical to BCAA supplements in appearance, odor, and packaging to maintain blinding.

    Dietary Supplement: The Placebo Group (control group) takes oral placebo for 3 months postoperatively-prepared by an independent third party, the placebo is identical to BCAA supplements in appearance, odor, and packagin

Interventions

  • Dietary supplementThe BCAA Group (experimental group) takes oral branched-chain amino acid (BCAA) supplements for 3 months starting after TIPS.

    This prospective randomized controlled trial (RCT) aims to compare changes in muscle mass and clinical outcomes between sarcopenic cirrhotic patients with portal hypertension and variceal bleeding who undergo transjugular intrahepatic portosystemic shunt (TIPS) plus branched-chain amino acid (BCAA) supplementation versus TIPS plus placebo. Eligible patients are aged 18-75 years, with cirrhosis, sarcopenia (defined by EASL guidelines: L3 skeletal muscle index \[L3-SMI\] \<50 cm²/m² for males, \<39 cm²/m² for females, measured via preoperative abdominal CT), and TIPS eligibility due to variceal bleeding or refractory ascites; exclusions include malignancies, severe cardiopulmonary insufficiency, Child-Pugh score \>13, recurrent hepatic encephalopathy (HE), and prior use of nutrition supplements within 3 months. TIPS is standardized with 8mm covered Viatorr stents, intraoperative variceal embolization if needed, and a postoperative portal pressure gradient (PPG) target of \<12 mmHg or ≥50% base

  • Dietary supplementThe Placebo Group (control group) takes oral placebo for 3 months postoperatively-prepared by an independent third party, the placebo is identical to BCAA supplements in appearance, odor, and packagin

    The Placebo Group (control group) takes oral placebo for 3 months postoperatively-prepared by an independent third party, the placebo is identical to BCAA supplements in appearance, odor, and packaging to maintain blinding.

06

What researchers measure

Primary outcomes

  1. Differences in the sarcopenia reversal rate between the two groups (BCAA and Non-BCAA)

    Sarcopenia is defined per the European Association for the Study of the Liver (EASL) clinical practice guidelines: the skeletal muscle index (SMI) is calculated as the ratio of the total cross-sectional area of all skeletal muscles at the third lumbar (L3) level (measured via abdominal CT, unit: cm²) to the square of height (unit: m²), with males having SMI \< 50 cm²/m² and females \< 39 cm²/m² diagnosed as sarcopenic. SMI is measured preoperatively and at 3 and 6 months post-TIPS to determine the reversal rate (proportion of patients no longer meeting sarcopenia criteria), and the difference in this rate between the two groups is compared to evaluate the effect of BCAA supplementation.

    Time frame: 1 year

  2. Differences in Short Physical Performance Battery (SPPB) scores between the two groups (BCAA and Non-BCAA)

    The SPPB consists of three subtests: balance test, gait speed test, and Chair Stand Test. Each subtest is scored from 0 to 4 points, with a total score ranging from 0 to 12 points-higher scores indicate better physical fitness. The SPPB is assessed preoperatively and at 3 and 6 months post-TIPS to compare changes in physical performance between the BCAA and Non-BCAA groups, reflecting the effect of BCAA supplementation on functional capacity in cirrhotic patients with sarcopenia.

    Time frame: 1 year

Secondary outcomes

  1. The cumulative incidence of hepatic encephalopathy (HE) in the two groups (BCAA and Non-BCAA)

    Hepatic encephalopathy (HE) is diagnosed and graded in accordance with the West-Haven criteria, with overt HE (OHE) defined as Grades II-IV. Data are collected during follow-up at 3 and 6 months after TIPS to compare whether branched-chain amino acid (BCAA) supplementation reduces the risk of HE compared with placebo. The Kaplan-Meier method is used to plot the cumulative incidence curves of HE in the two groups, and the Log-rank test is applied to compare the differences in the risk of HE occurrence between the two groups.

    Time frame: 1 year

  2. The cumulative incidence of death in the two groups (BCAA and Non-BCAA)

    Death is defined as all-cause mortality occurring during the follow-up period after TIPS. Data on mortality events (including the time and cause of death) are collected through regular follow-up assessments at 3 and 6 months post-TIPS, as well as active follow-up via medical records and telephone inquiries for any unplanned hospitalizations or death reports. The aim is to compare whether branched-chain amino acid (BCAA) supplementation reduces the risk of death compared with placebo. The Kaplan-Meier method is used to plot the cumulative survival curves (and corresponding cumulative mortality curves) of the two groups, and the Log-rank test is applied to compare the differences in mortality risk between the two groups.

    Time frame: 1 year

  3. The cumulative incidence of Variceal Rebleeding in the two groups (BCAA and Non-BCAA)

    Variceal rebleeding is diagnosed in accordance with the Baveno VII consensus criteria, defined as recurrent melena or hematemesis leading to any of the following: hospitalization, blood transfusion requirement, a decrease in hemoglobin of ≥3 g within 24 hours, or death within 6 weeks of the index bleeding event. Relevant data (including the time of rebleeding, clinical manifestations, and diagnostic evidence) are collected during scheduled follow-up at 3 and 6 months post-TIPS, as well as through emergency department and hospitalization records for acute bleeding episodes. The goal is to evaluate whether BCAA supplementation lowers the risk of variceal rebleeding compared with placebo. The Kaplan-Meier method is used to plot the cumulative incidence curves of variceal rebleeding in the two groups, and the Log-rank test is applied to compare the differences in rebleeding risk between the two groups.

    Time frame: 1 year

  4. The cumulative incidence of Shunt Dysfunction in the two groups (BCAA and Non-BCAA)

    Shunt dysfunction is diagnosed based on the following criteria: color Doppler ultrasound detects a maximum shunt tract blood flow velocity ≤50 cm/s, ≥200 cm/s, or no blood flow signal; or recurrence of clinical symptoms (such as variceal rebleeding or refractory ascites) suggestive of shunt malfunction, which is further confirmed by transjugular portography showing \>50% stenosis of the shunt tract. Data on shunt function are collected through color Doppler ultrasound examinations during follow-up at 3 and 6 months post-TIPS, as well as through portography for suspected cases. The purpose is to compare whether BCAA supplementation affects the risk of shunt dysfunction compared with placebo. The Kaplan-Meier method is used to plot the cumulative incidence curves of shunt dysfunction in the two groups, and the Log-rank test is applied to compare the differences in the risk of shunt dysfunction between the two groups.

    Time frame: 1 year

07

Study locations

1 of 1 sites recruiting
  • Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
    Wuhan, China
    Recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 15, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07281846
Lead sponsor
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Collaborators
The First Affiliated Hospital of Zhengzhou University, The First Affiliated Hospital of Henan University of Science and Technology
Responsible party
Jiacheng Liu (Clinical Investigator, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology) — Principal investigator
First posted
Dec 15, 2025
Start date
Nov 15, 2025
Primary completion
Nov 15, 2027 (estimated)
Completion
Nov 15, 2027 (estimated)
Last update
Dec 15, 2025

Study contacts

Yaowei Bai
Contact
baiyaowei918@163.com
+8618627162379

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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