SarcopeniaNCT04466709
The Relationship Betweensarcopenia And Myosteatosis With The Natural History Of Liver Cirrhosis
An observational study of Sarcopenia and Sarcopenic Obesity, run by University of Roma La Sapienza at 1 site in Italy.
Trial summary
Malnutrition is a common figure associated with liver cirrhosis. The main component of malnutrition in liver cirrhosis is represented by sarcopenia, a condition of a progressive and generalized loss of muscle mass and strength. Read more about this study
- Who is it for?
- Ages 40 to 75 years
- Conditions the study is for
- Sarcopenia, Sarcopenic Obesity, Cirrhosis, Liver
- What is being tested?
- none intervention type
- How many people
- 374 participants
- Where
- 1 siteItaly
- Study dates
- 10 Jul 2019to 1 Jan 2022
- Phase
- Observational
- 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 40 to 75 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: The sample size has been planned using results from an analogous retrospective study, where the HR for sarcopenia was estimated as 2.2, the 1-y event rate was 30%, and 40% of the sample had sarcopenia. We therefore conservatively assume a sHR equal to 2, 20% 1-y cause-specific event rate, 40% baseline sarcopenia. According to these data, a total of 68 cause-specific events are needed to guarantee the power of at least 80% with a type I error rate of 5%. Since we assume a 20% event rate, with a follow-up of 1y as planned 340 patients (68/0.2) will be enrolled. Considering a possible 10% drop-out, a total of 374 patients will be enrolled in the study.
Who may be able to join
- all patients with liver cirrhosis (age 40 - 75 years) undergoing abdominal CT-scan including the third lumbar L3 vertebrae for the clinical indication (surveillance of focal liver lesions, vascular evaluation, pre-transplant evaluation, pre-TIPS evaluation.) will be considered for the enrollment.
Who cannot join
- Active list for liver transplantation (LT) (patients at evaluation for LT will beenrolled);
- hepatocellular carcinoma HCC;
- previous LT or listing for multivisceral or living-related LT;
- concomitant neuromuscular disease;
- Patients with acute or subacute liver failure without underlying cirrhosis;
- Evidence of current malignancy except for non-melanocytic skin cancer;
Show all 9Show fewer
- Presence or history of severe extra-hepatic diseases (e.g., chronic renal failure requiring hemodialysis, severe heart disease (NYHA III-IV); severe chronic pulmonary disease (GOLD > III), severe neurological and psychiatric disorders);
- HIV-positive patients;
- Patients who decline to participate or who cannot provide prior written informed consent and when there is documented evidence that the patient has no legal surrogate decision maker and it appears unlikely that the patient will regain consciousness or sufficient ability to provide delayed informed consent;
Trial locations and contacts
1 site in 1 country.
Italy1 site, 1 recruiting
- Recruiting
Gastroenterology Department, Sapienza University of Rome
Rome, 00100
Manuela Merli, +39 06 49972002, manuela.merli@uniroma1.it
About this study
Malnutrition is a common figure associated with liver cirrhosis. The main component of malnutrition in liver cirrhosis is represented by sarcopenia, a condition of a progressive and generalized loss of muscle mass and strength. Many studies have reported that sarcopenia is an independent predictor of morbidity and mortality in cirrhotic patients.
Moreover, cirrhotic patients may develop simultaneous loss of skeletal muscle and gain of adipose tissue, culminating in a condition of "sarcopenic obesity".
Read more
As highlighted by a recent systematic review and meta-analysis [Van Vgut 2017] all the studies on the impact of sarcopenia/sarcopenic obesity and myosteatosis in cirrhotic patients are retrospective studies, mostly involving non-consecutive patients on the list for liver transplantation. Moreover, most of the studies were produced by non-European centers (Canadians,Americans, and Japanese) that published more papers on the same patient series. All these factors have led to a possible selection bias.
Furthermore, the methods used to evaluate sarcopenia and myosteatosis were not homogeneous (the entire muscle area, or area of the psoas or psoas diameter) as well as the cut-offs used.
For these reasons, we propose a multicentric observational prospective study aimed at analyzing the impact of sarcopenia, sarcopenic obesity and myosteatosis in cirrhotic patients not listed for liver transplantation.
Primary endpoint:
- Evaluation of the impact of sarcopenia on the mortality of cirrhotic patients not on the waiting list for liver transplantation.
Secondary end-point:
- Evaluation of the impact of sarcopenic obesity and myosteatosis on the mortality of cirrhotic patients not on the waiting list for liver transplantation.
- Evaluation of the impact of sarcopenia/sarcopenic obesity and myosteatosis on the development of complications (hepatic encephalopathy, bacterial infections, ascites, GI bleeding) in cirrhotic patients not on the waiting list for liver transplantation.
- Evaluation of the impact of sarcopenia/sarcopenic obesity and myosteatosis on the number of admissions and the days of hospitalization for such complications.
- Evaluation of the subcutaneous fat impact on mortality and morbidity of cirrhotic patients not on the waiting list for liver transplantation.
- Concordance analysis of the various methods used (different cut-off/area psoas vs. area of all muscles) for the diagnosis of sarcopenia through the analysis of CT scan.
Read the detailed description
Malnutrition is a common figure associated with liver cirrhosis with an incidence ranging from 5% to 99% of patients depending on the population studied and diagnostic tools used for the diagnosis [Amodio Hepatology 2013; Merli ESPEN; Merli 2013]. Several factors are involved in the pathogenesis of malnutrition in the patient with liver cirrhosis as an inadequate dietary intake, altered nutrient uptake and alterations in the use of the substrate due to liver disease [Tandon P 2017, Plauth M 2002]. Furthermore, a variety of acute events and complications can reduce then patient's ability to take care of their food intake [Plauth M2002]. Malnutrition is associated with an increased risk of mortality, higher prevalence of portal hypertension-related complications and infections, as well as longer in hospital stay [Merli 1996, Merli 2010, Merli 2013, Tandon P Liver Transplant 2012, Montano-Loza 2012].
The main component of malnutrition in liver cirrhosis is represented by sarcopenia, a condition of a progressive and generalized loss of muscle mass and strength [Dasarathy S 2012, Montano-Loza AJ 2012, Cruz-jentoft AJ 2010]. Many studies have reported that sarcopenia is an independent predictor of morbidity and mortality in cirrhotic patients [Merli 2013, Tandon P Liver Transplant 2012, Montano-Loza 2012].
Moreover, while overweight and obesity are endemic in Western countries, these conditions have been associated with the development of chronic liver disease, worsening of liver fibrosis and progression to cirrhosis [Everhart JE 2009; Raynard B 2002]; furthermore, the body mass index(BMI) has been considered an independent risk factor for the development of decompensation among cirrhotic patients of all causes [Berzigotti A 2010].
Cirrhotic patients may develop simultaneous loss of skeletal muscle and gain of adipose tissue, culminating in a condition of "sarcopenic obesity" [Montano-Loza AJ 2016]. This observation is relevant because, despite its important role in the prognosis of cirrhosis, sarcopenia in cirrhotic patients is frequently overlooked as body composition assessments can be challenging in cirrhotic patients with fluid retention or who are overweight or frankly obese [O'Brein 2008]. In addition, muscle depletion is characterized by both a reduction in muscle size and an increased proportion of intermuscular and intramuscular fat denominated 'myosteatosis' [Montano-Loza AJ 2016]. Myosteatosis increases with age and adiposity and it is associated with metabolic abnormalities, decreased strength and mobility [Montano-Loza AJ 2016, Correa-de-Araujo R 2017].
Montano-Loza and colleagues showed that cirrhotic patients with sarcopenic obesity or myosteatosis had worse median survival compared to those patients with normal body composition [Montano- Loza A J 2016]. In previous work, Kabori et al. demonstrated an association between myosteatosis and the prevalence of diabetes mellitus in patients undergoing hepatocellular carcinoma resection [Kaibori M 2015].
Assessment of sarcopenia and myosteatosis The European Consensus Statement has identified computed tomography (CT) as the gold standard for the detection of muscle wasting in clinical trials [Cruz-Jentoft 2010] nevertheless in clinical practice, the execution of CT and MRI is difficult to be justified only for quantifying muscle mass.
However, most cirrhotic patients have imaging for surveillance of focal liver lesions, hepatocellular carcinoma, vascular disease and pre-transplant evaluation [Dasarathy 2016]. CT is more commonly used as some software enables specific tissue demarcation using precise HU thresholds [Mitsiopoulos 1998]. There is excellent reliability between different software systems, with a good reproducibility between the software package [Irving 2007]. Although heterogeneity in the literature also exists about the abdominal muscles measured (psoas or total abdominal wall) and the site of measurements (third or fourth lumbar vertebra) [Carey 2017], the measurement of the abdominal muscle area at L3-L4 is considered the gold standard due to the relative independence from the activity level and water retention [Montano-Loza 2012].
CT images have been also the most utilized as a research tool to investigate myosteatosis. It is basically assessed indirectly using muscle attenuation calculated, leading to a close correlation with direct measurements of muscle lipid content [Machann et al., 2003; Larson-Meyer et al., 2006].
Muscle radiation attenuation is a radiological characteristic that can be measured with Hounsfield units (HU) [Goodpaster et al., 2000; Goodpaster, 2002]. When muscle cross-sectional area and attenuation are reported, the most common practice is to use pre-established HU ranges to define intermuscular fat (usually -190 to -30 HU) and muscle tissue (usually -29 HU to 150 HU) [Aubrey et al., 2014].
As highlighted by a recent systematic review and meta-analysis [Van Vgut 2017] all the abovementioned studies on the impact of sarcopenia/sarcopenic obesity and myosteatosis in cirrhotic patients are retrospective studies, mostly involving non-consecutive patients on the list for liver transplantation. Moreover, most of the studies were produced by non-European centers (Canadians,Americans, and Japanese) that published more papers on the same patient series. All these factors have led to a possible selection bias.
Furthermore, the methods used to evaluate sarcopenia and myosteatosis were not homogeneous (the entire muscle area, or area of the psoas or psoas diameter) as well as the cut-offs used.
AIMS and ENDPOINT For these reasons, we propose a multicentric observational prospective study aimed at analyzing the impact of sarcopenia, sarcopenic obesity and myosteatosis in cirrhotic patients not listed for liver transplantation.
Primary endpoint:
- Evaluation of the impact of sarcopenia on the mortality of cirrhotic patients not on the waiting list for liver transplantation.
Secondary end-point:
- Evaluation of the impact of sarcopenic obesity and myosteatosis on the mortality of cirrhotic patients not on the waiting list for liver transplantation.
- Evaluation of the impact of sarcopenia/sarcopenic obesity and myosteatosis on the development of complications (hepatic encephalopathy, bacterial infections, ascites, GI bleeding) in cirrhotic patients not on the waiting list for livertransplantation.
- Evaluation of the impact of sarcopenia/sarcopenic obesity and myosteatosis on the number of admissions and the days of hospitalization for such complications.
- Evaluation of the subcutaneous fat impact on mortality and morbidity of cirrhotic patients not on the waiting list for liver transplantation.
- Concordance analysis of the various methods used (different cut-off/area psoas vs. area of all muscles) for the diagnosis of sarcopenia through the analysis of CT scan.
PATIENTS Collection of a large national cohort of patients with liver cirrhosis not listed for liver transplantation, undergoing CT-scan abdomen based on different indications (with or without contrast). Each center needs to enroll at least 10 patients within 6 months for an estimate of at least 20 participating Italian centers.
INCLUSION CRITERIA: all patients with liver cirrhosis (age 40 - 75 years) undergoing abdominal CT-scan including the third lumbar L3 vertebrae for the clinical indication (surveillance of focal liver lesions, vascular evaluation, pre-transplant evaluation, pre-TIPS evaluation.) will be considered for the enrollment.
- Conditions
- Sarcopenia, Sarcopenic Obesity, Cirrhosis, Liver
- Being tested
- none intervention type
- Keywords
- sarcopenia, myosteatosis
- Medical subject headings
- Sarcopenia, Liver Cirrhosis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
none intervention typeOther
This is an observational study, no intervention
What is being measured
The primary outcome is the main question the study is designed to answer.
sarcopenia and mortality
Evaluation of the impact of sarcopenia on the mortality of cirrhotic patients not on the waiting list for liver transplantation.
Measured: 1 year
Secondary outcomes (3)
sarcopenic obesity/myosteatosis and mortality
Evaluation of the impact of sarcopenic obesity and myosteatosis on the mortality of cirrhotic patients not on the waiting list for liver transplantation.
Measured: 1 year
sarcopenia, sarcopenic obesity/myosteatosis and complication of liver disease
Evaluation of the impact of sarcopenia/sarcopenic obesity and myosteatosis on the development of complications (hepatic encephalopathy, bacterial infections, ascites, GI bleeding) in cirrhotic patients not on the waiting list for livertransplantation.
Measured: 1 year
Methods Concordance
Concordance analysis of the various methods used (different cut-off/area psoas vs. area of all muscles) for the diagnosis of sarcopenia through the analysis of CT scan.
Measured: 1 year
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted10 Jul 2020
- Study start10 Jul 2019
- Primary completion5 Jul 2020
- Study completion1 Jan 2022 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for SarcopeniaStudies of the same condition, open and under way.
- More trials run by University of Roma La SapienzaThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 374 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University of Roma La Sapienza
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Manuela Merli, University of Roma La Sapienza
- Investigators
- Manuela Merli, Professor, Principal investigator, Sapeinza University of Roma
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04466709
- Sponsor's protocol ID
- 5226
- Status last verified
- Jul 2020
- First submitted
- 7 Jul 2020
- Last updated
- 10 Jul 2020
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 10 Jul 2020. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Relationship Betweensarcopenia And Myosteatosis With The Natural History Of Liver Cirrhosis
- ClinicalTrials.gov ID
- NCT04466709
- Acronym / sponsor ID
- 5226
- Conditions
- Sarcopenia, Sarcopenic Obesity, Cirrhosis, Liver
- Keywords
- sarcopenia, myosteatosis
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 374 participants (estimated)
- Lead sponsor
- University of Roma La SapienzaUniversity, hospital or other
- Study start
- 10 Jul 2019 (actual)
- Primary completion
- 5 Jul 2020 (actual)
- Study completion
- 1 Jan 2022 (estimated)
- First posted
- 10 Jul 2020 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Malnutrition is a common figure associated with liver cirrhosis. The main component of malnutrition in liver cirrhosis is represented by sarcopenia, a condition of a progressive and generalized loss of muscle mass and strength. Many studies have reported that sarcopenia is an independent predictor of morbidity and mortality in cirrhotic patients.
Moreover, cirrhotic patients may develop simultaneous loss of skeletal muscle and gain of adipose tissue, culminating in a condition of "sarcopenic obesity".
As highlighted by a recent systematic review and meta-analysis [Van Vgut 2017] all the studies on the impact of sarcopenia/sarcopenic obesity and myosteatosis in cirrhotic patients are retrospective studies, mostly involving non-consecutive patients on the list for liver transplantation. Moreover, most of the studies were produced by non-European centers (Canadians,Americans, and Japanese) that published more papers on the same patient series. All these factors have led to a possible selection bias.
Furthermore, the methods used to evaluate sarcopenia and myosteatosis were not homogeneous (the entire muscle area, or area of the psoas or psoas diameter) as well as the cut-offs used.
For these reasons, we propose a multicentric observational prospective study aimed at analyzing the impact of sarcopenia, sarcopenic obesity and myosteatosis in cirrhotic patients not listed for liver transplantation.
Primary endpoint:
- Evaluation of the impact of sarcopenia on the mortality of cirrhotic patients not on the waiting list for liver transplantation.
Secondary end-point:
- Evaluation of the impact of sarcopenic obesity and myosteatosis on the mortality of cirrhotic patients not on the waiting list for liver transplantation.
- Evaluation of the impact of sarcopenia/sarcopenic obesity and myosteatosis on the development of complications (hepatic encephalopathy, bacterial infections, ascites, GI bleeding) in cirrhotic patients not on the waiting list for liver transplantation.
- Evaluation of the impact of sarcopenia/sarcopenic obesity and myosteatosis on the number of admissions and the days of hospitalization for such complications.
- Evaluation of the subcutaneous fat impact on mortality and morbidity of cirrhotic patients not on the waiting list for liver transplantation.
- Concordance analysis of the various methods used (different cut-off/area psoas vs. area of all muscles) for the diagnosis of sarcopenia through the analysis of CT scan.
Detailed description
Malnutrition is a common figure associated with liver cirrhosis with an incidence ranging from 5% to 99% of patients depending on the population studied and diagnostic tools used for the diagnosis [Amodio Hepatology 2013; Merli ESPEN; Merli 2013]. Several factors are involved in the pathogenesis of malnutrition in the patient with liver cirrhosis as an inadequate dietary intake, altered nutrient uptake and alterations in the use of the substrate due to liver disease [Tandon P 2017, Plauth M 2002]. Furthermore, a variety of acute events and complications can reduce then patient's ability to take care of their food intake [Plauth M2002]. Malnutrition is associated with an increased risk of mortality, higher prevalence of portal hypertension-related complications and infections, as well as longer in hospital stay [Merli 1996, Merli 2010, Merli 2013, Tandon P Liver Transplant 2012, Montano-Loza 2012].
The main component of malnutrition in liver cirrhosis is represented by sarcopenia, a condition of a progressive and generalized loss of muscle mass and strength [Dasarathy S 2012, Montano-Loza AJ 2012, Cruz-jentoft AJ 2010]. Many studies have reported that sarcopenia is an independent predictor of morbidity and mortality in cirrhotic patients [Merli 2013, Tandon P Liver Transplant 2012, Montano-Loza 2012].
Moreover, while overweight and obesity are endemic in Western countries, these conditions have been associated with the development of chronic liver disease, worsening of liver fibrosis and progression to cirrhosis [Everhart JE 2009; Raynard B 2002]; furthermore, the body mass index(BMI) has been considered an independent risk factor for the development of decompensation among cirrhotic patients of all causes [Berzigotti A 2010].
Cirrhotic patients may develop simultaneous loss of skeletal muscle and gain of adipose tissue, culminating in a condition of "sarcopenic obesity" [Montano-Loza AJ 2016]. This observation is relevant because, despite its important role in the prognosis of cirrhosis, sarcopenia in cirrhotic patients is frequently overlooked as body composition assessments can be challenging in cirrhotic patients with fluid retention or who are overweight or frankly obese [O'Brein 2008]. In addition, muscle depletion is characterized by both a reduction in muscle size and an increased proportion of intermuscular and intramuscular fat denominated 'myosteatosis' [Montano-Loza AJ 2016]. Myosteatosis increases with age and adiposity and it is associated with metabolic abnormalities, decreased strength and mobility [Montano-Loza AJ 2016, Correa-de-Araujo R 2017].
Montano-Loza and colleagues showed that cirrhotic patients with sarcopenic obesity or myosteatosis had worse median survival compared to those patients with normal body composition [Montano- Loza A J 2016]. In previous work, Kabori et al. demonstrated an association between myosteatosis and the prevalence of diabetes mellitus in patients undergoing hepatocellular carcinoma resection [Kaibori M 2015].
Assessment of sarcopenia and myosteatosis The European Consensus Statement has identified computed tomography (CT) as the gold standard for the detection of muscle wasting in clinical trials [Cruz-Jentoft 2010] nevertheless in clinical practice, the execution of CT and MRI is difficult to be justified only for quantifying muscle mass.
However, most cirrhotic patients have imaging for surveillance of focal liver lesions, hepatocellular carcinoma, vascular disease and pre-transplant evaluation [Dasarathy 2016]. CT is more commonly used as some software enables specific tissue demarcation using precise HU thresholds [Mitsiopoulos 1998]. There is excellent reliability between different software systems, with a good reproducibility between the software package [Irving 2007]. Although heterogeneity in the literature also exists about the abdominal muscles measured (psoas or total abdominal wall) and the site of measurements (third or fourth lumbar vertebra) [Carey 2017], the measurement of the abdominal muscle area at L3-L4 is considered the gold standard due to the relative independence from the activity level and water retention [Montano-Loza 2012].
CT images have been also the most utilized as a research tool to investigate myosteatosis. It is basically assessed indirectly using muscle attenuation calculated, leading to a close correlation with direct measurements of muscle lipid content [Machann et al., 2003; Larson-Meyer et al., 2006].
Muscle radiation attenuation is a radiological characteristic that can be measured with Hounsfield units (HU) [Goodpaster et al., 2000; Goodpaster, 2002]. When muscle cross-sectional area and attenuation are reported, the most common practice is to use pre-established HU ranges to define intermuscular fat (usually -190 to -30 HU) and muscle tissue (usually -29 HU to 150 HU) [Aubrey et al., 2014].
As highlighted by a recent systematic review and meta-analysis [Van Vgut 2017] all the abovementioned studies on the impact of sarcopenia/sarcopenic obesity and myosteatosis in cirrhotic patients are retrospective studies, mostly involving non-consecutive patients on the list for liver transplantation. Moreover, most of the studies were produced by non-European centers (Canadians,Americans, and Japanese) that published more papers on the same patient series. All these factors have led to a possible selection bias.
Furthermore, the methods used to evaluate sarcopenia and myosteatosis were not homogeneous (the entire muscle area, or area of the psoas or psoas diameter) as well as the cut-offs used.
AIMS and ENDPOINT For these reasons, we propose a multicentric observational prospective study aimed at analyzing the impact of sarcopenia, sarcopenic obesity and myosteatosis in cirrhotic patients not listed for liver transplantation.
Primary endpoint:
- Evaluation of the impact of sarcopenia on the mortality of cirrhotic patients not on the waiting list for liver transplantation.
Secondary end-point:
- Evaluation of the impact of sarcopenic obesity and myosteatosis on the mortality of cirrhotic patients not on the waiting list for liver transplantation.
- Evaluation of the impact of sarcopenia/sarcopenic obesity and myosteatosis on the development of complications (hepatic encephalopathy, bacterial infections, ascites, GI bleeding) in cirrhotic patients not on the waiting list for livertransplantation.
- Evaluation of the impact of sarcopenia/sarcopenic obesity and myosteatosis on the number of admissions and the days of hospitalization for such complications.
- Evaluation of the subcutaneous fat impact on mortality and morbidity of cirrhotic patients not on the waiting list for liver transplantation.
- Concordance analysis of the various methods used (different cut-off/area psoas vs. area of all muscles) for the diagnosis of sarcopenia through the analysis of CT scan.
PATIENTS Collection of a large national cohort of patients with liver cirrhosis not listed for liver transplantation, undergoing CT-scan abdomen based on different indications (with or without contrast). Each center needs to enroll at least 10 patients within 6 months for an estimate of at least 20 participating Italian centers.
INCLUSION CRITERIA: all patients with liver cirrhosis (age 40 - 75 years) undergoing abdominal CT-scan including the third lumbar L3 vertebrae for the clinical indication (surveillance of focal liver lesions, vascular evaluation, pre-transplant evaluation, pre-TIPS evaluation.) will be considered for the enrollment.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Ages
- 40 to 75 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- The sample size has been planned using results from an analogous retrospective study, where the HR for sarcopenia was estimated as 2.2, the 1-y event rate was 30%, and 40% of the sample had sarcopenia. We therefore conservatively assume a sHR equal to 2, 20% 1-y cause-specific event rate, 40% baseline sarcopenia. According to these data, a total of 68 cause-specific events are needed to guarantee the power of at least 80% with a type I error rate of 5%. Since we assume a 20% event rate, with a follow-up of 1y as planned 340 patients (68/0.2) will be enrolled. Considering a possible 10% drop-out, a total of 374 patients will be enrolled in the study.
Key inclusion criteria (1 listed)
- all patients with liver cirrhosis (age 40 - 75 years) undergoing abdominal CT-scan including the third lumbar L3 vertebrae for the clinical indication (surveillance of focal liver lesions, vascular evaluation, pre-transplant evaluation, pre-TIPS evaluation.) will be considered for the enrollment.
Key exclusion criteria (9 listed)
- Active list for liver transplantation (LT) (patients at evaluation for LT will beenrolled);
- hepatocellular carcinoma HCC;
- previous LT or listing for multivisceral or living-related LT;
- concomitant neuromuscular disease;
- Patients with acute or subacute liver failure without underlying cirrhosis;
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| none intervention typeThis is an observational study, no intervention | Other | – |
Primary outcome
sarcopenia and mortality
Time frame: 1 year
Evaluation of the impact of sarcopenia on the mortality of cirrhotic patients not on the waiting list for liver transplantation.
3 secondary outcomes
sarcopenic obesity/myosteatosis and mortality
Time frame: 1 year
sarcopenia, sarcopenic obesity/myosteatosis and complication of liver disease
Time frame: 1 year
Methods Concordance
Time frame: 1 year
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 10 Jul 2020.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Manuela Merli, Professor principal investigator
Sapeinza University of Roma
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Sarcopenia and Sarcopenic Obesity, run by University of Roma La Sapienza at 1 site in Italy.
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 1 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 10 Jul 2020. 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 Italy. 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.
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 Manuela Merli, Professor (0649972002, manuela.merli@uniroma1.it), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
sarcopenia and mortality (time frame: 1 year). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
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 10 Jul 2020.