Endoscopic Ultrasound Shear Wave vs Transient Elastography for Liver Steatosis: The RUMIPAMBA Trial

Sponsor
Instituto Ecuatoriano de Enfermedades Digestivas (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06102980
Collaborator
(none)
30
2
5

Study Details

Study Description

Brief Summary

Currently, there is no description of the contribution of the endoscopic ultrasound (EUS)-guided shear wave elastography (SWE) when describing liver steatosis in patients with suspicion of metabolic dysfunction-associated steatotic liver disease (MASLD). Similar research have been published but using vibration-controlled transient elastography (VCTE), recommended mainly due to its lower cost and less invasiveness. However, VCTE is limited to the anatomical proportions of the patient's body, and cannot assess the right hepatic lobe with less reliability, in opposition to the EUS-SWE.

Condition or Disease Intervention/Treatment Phase
  • Device: Transparietal ultrasound (US)-based shear wave elastography (SWE)
  • Device: Vibration-controlled transient elastography (VCTE)
  • Device: Endoscopic ultrasound (EUS)-guided shear wave elastography (SWE)
N/A

Detailed Description

Metabolic dysfunction-associated steatotic liver disease (MASLD), formerly non-alcoholic fatty liver disease (NAFLD), is an umbrella term which involves simple liver steatosis, metabolic-associated steatohepatitis (MASH) and MASH-related liver cirrhosis. Liver steatosis relies on imaging or biomarkers, but liver biopsy remains the gold standard for its diagnosis and grading. It comprehends intracellular accumulation of triacylglycerol (TAG) as microvascular or macrovascular lipid droplets in at least 5% of hepatocytes. Liver biopsy is invasive, requires a high-quality biopsy sample, can mislead a diagnosis due to sampling bias, depends on pathologist interpretation variability and implies adverse events related to punction.

There are non-invasive resources useful for liver steatosis screening and surveillance. Apart from serum biomarkers, non-invasive technologies designed for this purpose use ultrasound (US)-based elastography, namely: US strain, acoustic radiation force impulse (ARFI), point shear wave elastography (pSWE), two-dimension shear wave elastography (2D-SWE) and vibration-controlled transient elastography (VCTE). Although VCTE presents anatomical limitations when used in overweight patients or assessing the right hepatic lobe, it is largely accepted by international guidelines for assessing liver steatosis and fibrosis. Endoscopic ultrasound (EUS)-guided shear wave elastography (SWE) is independent of patients' anatomical proportions, and it permits a more reliable right hepatic lobe evaluation. However, it is an invasive and high-cost procedure.

VCTE and EUS-SWE determine liver steatosis quantitatively through the controlled attenuation parameter (CAP) and the attenuation coefficient (ATT), respectively. The ATT is equivalent to the CAP, both expressed in decibels per meter [dB/m]. There are four important gaps in the literature. First, the diagnostic accuracy of VCTE for liver steatosis has been profoundly analysed in NAFLD, but in a wide spectrum of liver fibrosis patients, from absent to cirrhosis. These limits finding extrapolations for screening and surveillance. Second, comparisons between EUS-SWE vs. VCTE have concentrated on liver fibrosis or cirrhosis. Third, there is no determined diagnostic accuracy for liver steatosis through EUS-SWE, each day more requested procedures are. Finally, as a new proposed term, liver steatosis identification and grading still need to be described in the nowadays called MASLD patients. The present study aims to compare MASLD-related liver steatosis estimation using CAP of the VCTE and the ATT of the EUS-SWE, comparing controls vs. liver steatosis patients with absent or mild liver fibrosis determined through non-invasive methods.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
30 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Investigator, Outcomes Assessor)
Masking Description:
After EUS-SWE, a clinical research coordinator will open the label to confirm the patient's cohort. The patient will undergo the EUS-guided two-lobe liver biopsy only if the patient belongs to the liver steatosis group.
Primary Purpose:
Diagnostic
Official Title:
Liver Steatosis Through Endoscopic Ultrasound-guided Shear Wave Elastography vs Vibration-controlled Transient Elastography: a Blinded Diagnostic Trial in Noninvasive Methods-determined Absent-to-mild Liver Fibrosis: The RUMIPAMBA Trial
Anticipated Study Start Date :
Nov 1, 2023
Anticipated Primary Completion Date :
Dec 1, 2023
Anticipated Study Completion Date :
Apr 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Liver steatosis

Patients with requirements of screening following the European Association for the Study of the Liver (EASL) 2016 recommendations. The liver steatosis group will be compounded by patients with at least one of the following criteria: Over fifty years old; Body mass index (BMI) over 25 kg/m2; Diabetes mellitus type 2; Metabolic syndrome; or Persistently elevated liver enzymes.

Device: Transparietal ultrasound (US)-based shear wave elastography (SWE)
The operator will be blinded to any clinical record. Before US-SWE, the patient must be fasted for a minimum of 4 hours and must remain alcohol-free for 7 days. Using an Aloka Arietta 850 (Olympus America, PA, USA), each patient must be supine. Upon breath-hold at the end of expiration, ten measurements will be obtained with the probe placed in the area of the right hepatic lobe through an intercostal space.
Other Names:
  • US-SWE
  • Device: Vibration-controlled transient elastography (VCTE)
    The operator will be blinded to any clinical record. Before VCTE, the patient must be fasted for a minimum of 4 hours and must remain alcohol-free for 7 days. Using the FibroScan® Compact 530 (Echosens, Paris, France), each patient must be supine with the right arm in abduction and the ipsilateral hand resting under the head. Upon breath-hold at the end of expiration, ten measurements will be obtained with the M-probe placed in the area of the right hepatic lobe through an intercostal space. Transition to an XL probe will be based on a VCTE automatic probe selection tool prompt.
    Other Names:
  • VCTE
  • Device: Endoscopic ultrasound (EUS)-guided shear wave elastography (SWE)
    EUS-SWE will be performed by an experienced endoscopist, who will be blinded to any clinical records. The expert will use the ArrietaTM 850 EUS console (Fujifilm, Tokyo, Japan) using a linear ultrasound video gastroscope EUS-J10 (Pentax Medical, Hoya Corp, Japan). The patient must be lying in the supine position. Based on the premise that as fibrosis progresses the distribution becomes heterogeneous, both lobes will be evaluated. The transducer will be positioned in the gastric window to visualize right liver segment number five and left liver segment two or three. After the patient suspended respiration for a few seconds, the elastogram region of interest (ROI) will be placed within the liver tissue at a distance ≥10 mm beneath the hepatic capsule in an area free of vessels and artefacts. A 10-mm circular ROI will be placed within the elastogram at a depth of 4-5 cm from the skin, and a minimum of ten successful kPa measurements will be obtained.
    Other Names:
  • EUS-SWE
  • Other: Controls

    Patients without requirements of screening following the European Association for the Study of the Liver (EASL) 2016 recommendations. The liver steatosis group will be compounded by patients who will not present any of the following criteria: Over fifty years old; Body mass index (BMI) over 25 kg/m2; Diabetes mellitus type 2; Metabolic syndrome; and Persistently elevated liver enzymes. To be a control participant does not mean that the patient is a healthy participant. The control participants are patients who request any type of endoscopy and fulfil the criteria not to screen for liver steatosis. For example, a 48-year-old male with 21 kg/m2 BMI, without diabetes mellitus type 2, any metabolic syndrome-related comorbidities, with normal liver enzymes and who refused an episode of persistently elevated liver enzymes, with persistent reflux disease after two months of proton pump inhibitor therapy,

    Device: Transparietal ultrasound (US)-based shear wave elastography (SWE)
    The operator will be blinded to any clinical record. Before US-SWE, the patient must be fasted for a minimum of 4 hours and must remain alcohol-free for 7 days. Using an Aloka Arietta 850 (Olympus America, PA, USA), each patient must be supine. Upon breath-hold at the end of expiration, ten measurements will be obtained with the probe placed in the area of the right hepatic lobe through an intercostal space.
    Other Names:
  • US-SWE
  • Device: Vibration-controlled transient elastography (VCTE)
    The operator will be blinded to any clinical record. Before VCTE, the patient must be fasted for a minimum of 4 hours and must remain alcohol-free for 7 days. Using the FibroScan® Compact 530 (Echosens, Paris, France), each patient must be supine with the right arm in abduction and the ipsilateral hand resting under the head. Upon breath-hold at the end of expiration, ten measurements will be obtained with the M-probe placed in the area of the right hepatic lobe through an intercostal space. Transition to an XL probe will be based on a VCTE automatic probe selection tool prompt.
    Other Names:
  • VCTE
  • Device: Endoscopic ultrasound (EUS)-guided shear wave elastography (SWE)
    EUS-SWE will be performed by an experienced endoscopist, who will be blinded to any clinical records. The expert will use the ArrietaTM 850 EUS console (Fujifilm, Tokyo, Japan) using a linear ultrasound video gastroscope EUS-J10 (Pentax Medical, Hoya Corp, Japan). The patient must be lying in the supine position. Based on the premise that as fibrosis progresses the distribution becomes heterogeneous, both lobes will be evaluated. The transducer will be positioned in the gastric window to visualize right liver segment number five and left liver segment two or three. After the patient suspended respiration for a few seconds, the elastogram region of interest (ROI) will be placed within the liver tissue at a distance ≥10 mm beneath the hepatic capsule in an area free of vessels and artefacts. A 10-mm circular ROI will be placed within the elastogram at a depth of 4-5 cm from the skin, and a minimum of ten successful kPa measurements will be obtained.
    Other Names:
  • EUS-SWE
  • Outcome Measures

    Primary Outcome Measures

    1. Vibration-controlled transient elastrography (VCTE) liver steatosis grade [Six months]

      Liver steatosis will be defined by elastography using the controlled attenuation parameter (CAP), measured in decibels per meter [db/m].

    2. Transparietal ultrasound (US)-based shear wave elastography (SWE) liver steatosis grade [Six months]

      Liver steatosis will be defined by elastography using the attenuation coefficient (ATT), measured in decibels per meter [db/m]. The ATT corresponds to the VCTE CAP measurement.

    3. Endoscopic ultrasound (EUS)-guided shear wave elastography (SWE) liver steatosis grade [Six months]

      Liver steatosis per hepatic lobe will be defined by elastography using the attenuation coefficient (ATT) measurement [db/m]. The ATT corresponds to the VCTE CAP measurement.

    4. Endoscopic ultrasound (EUS)-guided liver biopsy steatosis grade [Six months]

      The EUS-guided liver biopsy findings, per hepatic lobe, will be standardised through the steatosis-Activity-Fibrosis (SAF) score.

    Secondary Outcome Measures

    1. Vibration-controlled transient elastrography (VCTE) liver fibrosis grade [Six months]

      Liver steatosis will be defined by elastography using kilopascals [kPa].

    2. Transparietal ultrasound (US)-based shear wave elastography (SWE) liver fibrosis grade [Six months]

      Liver steatosis will be defined by elastography using kilopascals [kPa].

    3. Endoscopic ultrasound (EUS)-guided shear wave elastography (SWE) liver fibrosis grade [Six months]

      Liver steatosis per hepatic lobe will be defined by elastography using kilopascals [kPa].

    4. Endoscopic ultrasound (EUS)-guided liver biopsy fibrosis grade [Six months]

      The EUS-guided liver biopsy findings, per hepatic lobe, will be standardised through the Brunt system.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 79 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patients referred for any kind of endoscopic procedure.

    • Without clinical suspicion of advanced liver fibrosis.

    • Acceptance to participate in the study.

    Exclusion Criteria:
    • History of greater amounts of alcohol per week (140 g/week and 210 g/week for females and males respectively).

    • Significant or advanced fibrosis in accordance with FIB4 or APRI scores.

    • Any liver space-occupying lesion in the US.

    • Comorbidities or conditions related to avoidance of interventional procedures, namely: pregnancy or nursing, coagulopathy or any risk of bleeding, ASA IV or higher, NYHA III or IV.

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Instituto Ecuatoriano de Enfermedades Digestivas

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Carlos Robles-Medranda, Head of the Endoscopy Division, Instituto Ecuatoriano de Enfermedades Digestivas
    ClinicalTrials.gov Identifier:
    NCT06102980
    Other Study ID Numbers:
    • IECED-02102023
    First Posted:
    Oct 26, 2023
    Last Update Posted:
    Oct 26, 2023
    Last Verified:
    Oct 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    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
    Keywords provided by Carlos Robles-Medranda, Head of the Endoscopy Division, Instituto Ecuatoriano de Enfermedades Digestivas
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 26, 2023