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Body Composition Changes After TIPS and Associated Clinical Outcomes

Primary Purpose

Cirrhosis, Liver, Sarcopenia

Status
Recruiting
Phase
Early Phase 1
Locations
United States
Study Type
Interventional
Intervention
Transjugular Intrahepatic Portosystemic Shunt (TIPS) creation
Sponsored by
Oregon Health and Science University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cirrhosis, Liver focused on measuring cirrhosis, liver transplantation, sarcopenia, frailty

Eligibility Criteria

18 Years - 99 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 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

Exclusion Criteria:

  • 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
  • Decisionally impaired individuals
  • Need for emergency TIPS creation
  • Patients who do not have acceptable alternatives to TIPS creation to manage their disease

Sites / Locations

  • Oregon Health and Science UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

TIPS

Standard of care

Arm Description

Patients in this arm will undergo TIPS creation in addition to their current management.

Patients in this arm will continue to be treated with their current management

Outcomes

Primary Outcome Measures

Body composition changes
Muscle and fat content as assessed by CT scan
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.
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.

Secondary Outcome Measures

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).
Overall survival
Survival time
Transplant complications
Complications while on transplant waitlist as well as after transplant
Cardiac function
Right and left ventricular function noted by echocardiography
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)]
Cardiac mass
Myocardial mass as measured by echocardiography
Serum ammonia
serum ammonia level (micromol/L)
Serum glucose
serum glucose level (mg/dL)

Full Information

First Posted
May 6, 2022
Last Updated
June 13, 2022
Sponsor
Oregon Health and Science University
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1. Study Identification

Unique Protocol Identification Number
NCT05420753
Brief Title
Body Composition Changes After TIPS and Associated Clinical Outcomes
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
Study Type
Interventional

2. Study Status

Record Verification Date
June 2022
Overall Recruitment Status
Recruiting
Study Start Date
May 1, 2022 (Actual)
Primary Completion Date
February 2025 (Anticipated)
Study Completion Date
February 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Oregon Health and Science University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief 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. 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.
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cirrhosis, Liver, Sarcopenia
Keywords
cirrhosis, liver transplantation, sarcopenia, frailty

7. Study Design

Primary Purpose
Treatment
Study Phase
Early Phase 1
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
22 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
TIPS
Arm Type
Experimental
Arm Description
Patients in this arm will undergo TIPS creation in addition to their current management.
Arm Title
Standard of care
Arm Type
No Intervention
Arm Description
Patients in this arm will continue to be treated with their current management
Intervention Type
Procedure
Intervention Name(s)
Transjugular Intrahepatic Portosystemic Shunt (TIPS) creation
Intervention Description
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.
Primary Outcome Measure Information:
Title
Body composition changes
Description
Muscle and fat content as assessed by CT scan
Time Frame
Start to 2 years after enrollment
Title
Short Performance Physical Battery test
Description
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.
Time Frame
Start to 6 months after enrollment
Title
Liver Frailty test
Description
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.
Time Frame
Start to 6 months after enrollment
Secondary Outcome Measure Information:
Title
Chronic Liver Disease Quality of Life Questionnaire
Description
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).
Time Frame
Start to 6 months after enrollment
Title
Overall survival
Description
Survival time
Time Frame
Start to 2 years after enrollment
Title
Transplant complications
Description
Complications while on transplant waitlist as well as after transplant
Time Frame
Start to 30 days after transplant
Title
Cardiac function
Description
Right and left ventricular function noted by echocardiography
Time Frame
Start to 6 months after enrollment
Title
Liver function tests
Description
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)]
Time Frame
Start to 6 months after enrollment
Title
Cardiac mass
Description
Myocardial mass as measured by echocardiography
Time Frame
start to 6 months after enrollment
Title
Serum ammonia
Description
serum ammonia level (micromol/L)
Time Frame
start to 6 months after enrollment
Title
Serum glucose
Description
serum glucose level (mg/dL)
Time Frame
start to 6 months after enrollment
Other Pre-specified Outcome Measures:
Title
Stool microbiome genomic assessment
Description
Stool sample using DNAGenotek Omni-gene Stool collection kit to assess for bacterial complement in stool
Time Frame
Start to 6 months after enrollment
Title
Lipocalin-2 biomarker assessment
Description
Lipocalin-2 transcription and expression (RNA sequencing/Elisa/Western Blot) in serum samples
Time Frame
Start to 6 months after enrollment
Title
IL-6 biomarker assessment
Description
IL-6 immunoassay assessment of serum (pg/mL)
Time Frame
Start to 6 months after enrollment
Title
Salivary cortisol biomarker assessment
Description
salivary cortisol (mmol/L)
Time Frame
Start to 6 months after enrollment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 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 Exclusion Criteria: 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 Decisionally impaired individuals Need for emergency TIPS creation Patients who do not have acceptable alternatives to TIPS creation to manage their disease
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Khashayar Farsad, MD
Phone
503-494-7660
Email
farsad@ohsu.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Lori Russell, RN
Phone
503-494-7660
Email
watsonlo@ohsu.edu
Facility Information:
Facility Name
Oregon Health and Science University
City
Portland
State/Province
Oregon
ZIP/Postal Code
97239
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Khashayar Farsad, MD
Phone
503-494-7660
Email
farsad@ohsu.edu
First Name & Middle Initial & Last Name & Degree
Lori Russell, RN
Phone
503-494-7660
Email
watsonlo@ohsu.edu

12. IPD Sharing Statement

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Body Composition Changes After TIPS and Associated Clinical Outcomes

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