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Cirrhosis, LiverEarly Phase 1NCT05420753

Body Composition Changes After TIPS and Associated Clinical Outcomes

A Early Phase 1 study testing Transjugular Intrahepatic Portosystemic Shunt (TIPS) creation in people with Cirrhosis, Liver and Sarcopenia, run by Oregon Health and Science University at 1 site in United States.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

The purpose of this study is to prospectively assess the impact of TIPS creation on muscle mass and physical function in patients with cirrhosis, and to determine whether these changes correlate with improved outcomes in patients awaiting liver transplantation. Read more about this study

Who is it for?
Ages 18 to 99 years
Conditions the study is for
Cirrhosis, Liver, Sarcopenia
What is being tested?
Transjugular Intrahepatic Portosystemic Shunt (TIPS) creation
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
22 participants
Where
1 siteUnited States
Study dates
1 May 2022to 31 Dec 2025
Phase
Early Phase 1
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 99 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Patients >18 <99 with cirrhosis wait listed for liver transplantation
  • Evidence of complications of portal hypertension:
  • Ascites or hydrothorax requiring escalation of diuretic medication
  • Persistent ascites or hydrothorax despite diuretic use, or intolerance of diuretic use
  • Gastrointestinal varices and blood loss anemia or history of variceal hemorrhage
  • Portal hypertensive gastropathy and blood loss anemia
  • Chronic portal vein thrombosis requiring recanalization and TIPS for transplant

Who cannot join

  • Hepatocellular carcinoma or other active malignancy
  • Recurrent overt hepatic encephalopathy
  • Uncontrolled coagulopathy with maximum amplitude (MA) <30 on thromboelastography
  • Bacteremia or sepsis
  • MELD > 25
  • Pregnant
Show all 9Show fewer
  • Decisionally impaired individuals
  • Need for emergency TIPS creation
  • Patients who do not have acceptable alternatives to TIPS creation to manage their disease

Trial locations and contacts

1 site in 1 country.

Khashayar Farsad, MD contact

503-494-7660

farsad@ohsu.edu

Lori Russell, RN contact

503-494-7660

watsonlo@ohsu.edu

United States1 site, 1 recruiting
  • Oregon Health and Science University

    Portland, Oregon, 97239

    Khashayar Farsad, MD, 503-494-7660, farsad@ohsu.edu

    Lori Russell, RN, 503-494-7660, watsonlo@ohsu.edu

    Recruiting

Other trials in United States

About this study

Official title: Single-center Randomized Controlled Trial to Evaluate Body Composition Changes and Clinical Outcomes After Transjugular Intrahepatic Portosystemic Shunt (TIPS) Creation in Patients With Cirrhosis and Complications of Portal Hypertension Awaiting Liver Transplantation

The purpose of this study is to prospectively assess the impact of TIPS creation on muscle mass and physical function in patients with cirrhosis, and to determine whether these changes correlate with improved outcomes in patients awaiting liver transplantation. Retrospective observational studies have shown improvement in muscle mass and body composition in cirrhotic patients undergoing TIPS. The investigators aim to now prospectively study this through a pilot randomized controlled trial tracking patients managed with TIPS creation compared to those managed without TIPS to determine whether these observational findings can be seen in a randomized cohort. The investigators hypothesize that TIPS creation will lead to improved muscle mass, body composition and muscle function within the first 12 months after the procedure compared to a control group without TIPS, and that these changes will improve liver disease outcomes in patients awaiting liver transplantation.

Read the detailed description

Sarcopenia (loss of muscle mass) and frailty (loss of muscle function) have increasingly become recognized as major prognostic factors in predicting morbidity and mortality with several disease states, including cirrhosis. Cirrhosis represents end-stage liver disease and is complicated by a multitude of clinical sequelae, such as variceal hemorrhage, ascites, renal insufficiency, hepatic encephalopathy, hepatopulmonary syndrome, cardiac dysfunction, infection and hepatocellular carcinoma. To date, liver transplantation remains the only prospect for a curative treatment. As the liver is the primary metabolic organ, sarcopenia is prevalent in cirrhosis, afflicting 30-70% of patients. Observational studies have implicated sarcopenia as an independent risk factor for morbidity and mortality in all clinical sequelae of cirrhosis. Moreover, sarcopenia and frailty have been shown to increase morbidity and mortality of transplant eligible patients on the liver transplant waitlist, as well as mortality of patients after liver transplant. Given the prevalence of sarcopenia and frailty in this patient population, and the severe clinical impacts, addressing these adverse predictors may have profound implications for the outcomes of patients with cirrhosis.

Cirrhosis often leads to portal hypertension, complications of which include lower extremity edema, ascites, hepatic hydrothorax, variceal bleeding, portal hypertensive gastropathy, portal vein thrombosis, and hepatic encephalopathy. Patients with cirrhosis and complications of portal hypertension are currently managed in several ways in clinical practice:

  • medical management, including diuretics and non-selective beta blocker therapy
  • endoscopic options include variceal banding or glue embolization
  • invasive options include large-volume paracentesis (LVP) or transjugular intrahepatic portosystemic shunt (TIPS) creation.

Since 1988, the Liver Transplant Program at OHSU has been successfully treating waitlisted cirrhotic patients with complications of portal hypertension using a combination of these therapies. TIPS creation, particularly in the current era of stent grafts with a dedicated device for this procedure, has been a part of managing patients with cirrhosis as a bridge to transplant for two decades. Depending on the indication, patients can be treated with a combination of these therapies often with significant overlap. For example, a given patient with portal hypertension and ascites may be managed with diuretics and serial LVP vs. TIPS creation, and a given patient with variceal bleeding may be treated with beta-blockers and endoscopic banding vs. TIPS creation.

Of relevance to the proposed trial, recent observational studies have demonstrated significant reversal of sarcopenia after TIPS creation, and this reversal has been strongly correlated with improved survival and less hepatic encephalopathy. Moreover, the time course of muscle gains has been observed to occur within the first 6 months of TIPS creation, critical for patients awaiting liver transplantation, as benefits would occur during typical transplant waitlist time periods. Thus, TIPS creation may represent a major unmet need to address sarcopenia and frailty in patients with cirrhosis, and represents an intervention with potential to reverse this debilitating condition and improve clinical outcomes. Putative mechanisms for how TIPS creation may improve body composition include decreased congestive enteropathy resulting in improved gut nutrient absorption, decrease in metabolic burden from a hyperdynamic cardiopulmonary status in the setting of fluid overload, improvement in renal function, and changes in the gut microbiome resulting in conversion from a catabolic to an anabolic state. A major gap in knowledge, however, remains whether TIPS creation can directly reverse muscle loss. Furthermore, whether reversal of muscle loss results in improved measures of strength, physical performance and clinical outcomes has not been prospectively studied. In this proposal, the investigators plan to address this major knowledge gap through a pilot prospective randomized controlled trial tracking patients managed with TIPS creation compared to those managed without TIPS to determine whether these observational findings can be seen in a randomized cohort.

Being tested
Transjugular Intrahepatic Portosystemic Shunt (TIPS) creation
Keywords
cirrhosis, liver transplantation, sarcopenia, frailty
Medical subject headings
Liver Cirrhosis, Sarcopenia, Fibrosis, Frailty

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Transjugular Intrahepatic Portosystemic Shunt (TIPS) creationProcedure or surgery

    During a TIPS procedure, the interventional radiologist, with the help of x-ray and ultrasound guidance, makes a channel through the liver to connect the portal vein (the vein that carries blood from the digestive organs to the liver) to one of the hepatic vein (three veins that carry blood away from the liver back to the heart) using a special type of needle. The interventional radiologist then replaces the needle with a wire and catheter, and a small tubular device called a stent graft is placed in this channel to keep the pathway open between the two blood vessels.

Study groups in NCT05420753
Study groupRoleWhat they receive
TIPSExperimentalPatients in this arm will undergo TIPS creation in addition to their current management.
Receives: Procedure: Transjugular Intrahepatic Portosystemic Shunt (TIPS) creation
Standard of careNo interventionPatients in this arm will continue to be treated with their current management

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Body composition changes

    Muscle and fat content as assessed by CT scan

    Measured: Start to 2 years after enrollment

  2. Short Performance Physical Battery test

    Brief physical test for balance with feet together (seconds), gait speed walking 4 meters (seconds), time to stand from a chair (seconds). These are aggregated together to a unified score.

    Measured: Start to 6 months after enrollment

  3. Liver Frailty test

    Brief physical test for balance with feet together (seconds), time to stand from a chair (seconds), and grip strength (kilograms of force). These are aggregated together to a unified score.

    Measured: Start to 6 months after enrollment

Secondary outcomes (8)
  1. Chronic Liver Disease Quality of Life Questionnaire

    Quality of life assessment using 29 questions regarding experience of various symptoms graded on a scale of 1-7 each, with 1 being worse (all of the time) and 7 being the best (none of the time).

    Measured: Start to 6 months after enrollment

  2. Overall survival

    Survival time

    Measured: Start to 2 years after enrollment

  3. Transplant complications

    Complications while on transplant waitlist as well as after transplant

    Measured: Start to 30 days after transplant

  4. Cardiac function

    Right and left ventricular function noted by echocardiography

    Measured: Start to 6 months after enrollment

  5. Liver function tests

    Serum tests for total bilirubin (mg/dL), albumin (g/dL), sodium (mmol/L), creatinine (mg/dL), international normalized ratio. These values will be combined in the MELD score = 3.78×ln[serum bilirubin (mg/dL)] + 11.2×ln[INR] + 9.57×ln[serum creatinine (mg/dL)] + 6.43, and MELD-Na score = MELD + 1.32 x (137 - Na) - [0.033 x MELD*(137 - Na)]

    Measured: Start to 6 months after enrollment

  6. Cardiac mass

    Myocardial mass as measured by echocardiography

    Measured: start to 6 months after enrollment

  7. Serum ammonia

    serum ammonia level (micromol/L)

    Measured: start to 6 months after enrollment

  8. Serum glucose

    serum glucose level (mg/dL)

    Measured: start to 6 months after enrollment

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted15 Jun 2022
  2. Study start1 May 2022
  3. Primary completion31 Dec 2025 (estimated)
  4. Study completion31 Dec 2025 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Early Phase 1
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
22 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05420753
Sponsor's protocol ID
STUDY00022853
Status last verified
Nov 2023
First submitted
6 May 2022
Last updated
7 Nov 2023
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No

Publications

  • Suzuki T, Yamada K, Anoushiravani A, Pham P, Grossberg AJ, Naugler WE, Farsad K. Elective Transjugular Intrahepatic Portosystemic Shunt Creation in Cirrhosis Improves Body Composition and Function: Pilot Randomized Trial. Cardiovasc Intervent Radiol. 2026 Jun;49(6):1152-1162. doi: 10.1007/s00270-026-04405-7. Epub 2026 Mar 10.

    PubMed 41805969

Questions about this trial

What is this clinical trial studying?

A Early Phase 1 study testing Transjugular Intrahepatic Portosystemic Shunt (TIPS) creation in people with Cirrhosis, Liver and Sarcopenia, run by Oregon Health and Science University at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 7 Nov 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Early Phase 1 (sometimes called Phase 0) studies give a very small amount of a treatment to a few people, mainly to see how the body handles it.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Khashayar Farsad, MD (503-494-7660, farsad@ohsu.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Body composition changes (time frame: Start to 2 years after enrollment). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT05420753, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 7 Nov 2023.

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