- ICH GCP
- Yhdysvaltain kliinisten tutkimusten rekisteri
- Kliininen tutkimus NCT07714941
EUS-Guided ATI and SWE in Individuals With Normal FibroScan (EUS ATI&SWE)
"EUS-Guided Attenuation Imaging and Shear Wave Elastography in Individuals With Normal FibroScan: Establishing Preliminary Reference Values in a Pilot Feasibility Study".
The goal of this observational study is to establish preliminary reference values for Endoscopic Ultrasound (EUS)-guided Attenuation Imaging (ATI) and Shear Wave Elastography (SWE) in adults undergoing diagnostic EUS for non-hepatobiliary indications who have normal FibroScan findings. The main questions it aims to answer are:
What are the preliminary normal reference values for EUS-guided ATI in the right and left hepatic lobes? What are the preliminary normal reference values for EUS-guided SWE elasticity (kPa) and velocity (m/s) in the right and left hepatic lobes?
Participants will:
Undergo same-day FibroScan assessment to confirm normal liver stiffness and steatosis parameters.
Undergo EUS-guided ATI and SWE measurements of both the right and left hepatic lobes during their clinically indicated diagnostic EUS examination.
Have demographic, clinical, and laboratory information recorded for analysis.
Tutkimuksen yleiskatsaus
Tila
Yksityiskohtainen kuvaus
Vibration-controlled transient elastography (FibroScan) with Liver Stiffness Measurement (LSM) and Controlled Attenuation Parameter (CAP) is widely used for the non-invasive assessment of liver fibrosis and steatosis. Although these techniques have demonstrated good diagnostic performance, they have several limitations, including technical failure in obese individuals, reduced accuracy in the presence of ascites or narrow intercostal spaces, and the inability to obtain real-time image-guided measurements from specific areas of the liver.
Endoscopic ultrasound (EUS) provides high-resolution imaging of both hepatic lobes through the stomach and duodenum, allowing quantitative assessment of liver tissue under direct visualization. Recent advances have enabled the integration of Attenuation Imaging (ATI), which quantifies hepatic steatosis, and Shear Wave Elastography (SWE), which measures liver stiffness by estimating tissue elasticity and shear wave velocity, into EUS platforms. These techniques may overcome several limitations of conventional transabdominal elastography and have the potential to provide more reliable liver tissue characterization.
Before EUS-guided ATI and SWE can be evaluated as diagnostic tools for liver disease, normal reference values in individuals without liver disease must be established. Currently, there are limited data regarding normal EUS-guided ATI and SWE measurements, particularly in healthy adults with normal FibroScan findings. Establishing these reference ranges is essential for interpreting future studies involving patients with hepatic steatosis and chronic liver disease.
This prospective, single-center, observational pilot feasibility study aims to establish preliminary reference values for EUS-guided ATI and SWE in adults undergoing diagnostic EUS for non-hepatobiliary indications who have normal FibroScan examinations. A total of 100 participants will be enrolled after confirming normal liver stiffness (LSM <7.5 kPa) and steatosis (CAP <238 dB/m), along with adequate FibroScan quality criteria.
During the clinically indicated EUS examination, quantitative liver assessment will be performed without introducing additional invasive procedures beyond standard EUS. Attenuation Imaging will be obtained from both the right and left hepatic lobes, with five valid measurements acquired per lobe. Shear Wave Elastography will also be performed in both lobes, with ten valid measurements obtained per lobe. Measurements will be accepted only if predefined quality criteria are met, including acceptable correlation coefficients, propagation maps, and reliability indices. Acquisition time, technical success, and measurement reproducibility will also be recorded.
The primary outcome of the study is to establish preliminary reference values for EUS-guided ATI, SWE elasticity (kPa), and SWE velocity (m/s) for both hepatic lobes. Secondary objectives include evaluating the technical feasibility and reliability of EUS-guided quantitative liver assessment, assessing agreement between right and left hepatic lobe measurements, determining correlations between ATI and FibroScan CAP, evaluating correlations between SWE and FibroScan LSM, and documenting acquisition times for both techniques.
The findings from this pilot study will provide foundational reference data for EUS-guided quantitative liver imaging and support the design of larger validation studies investigating the role of EUS-guided ATI and SWE in the diagnosis and monitoring of hepatic steatosis and fibrosis.
Opintotyyppi
Ilmoittautuminen (Arvioitu)
Yhteystiedot ja paikat
Opiskeluyhteys
- Nimi: Aig research
- Puhelinnumero: +919182645727
- Sähköposti: aigresearch7@gmail.com
Opiskelupaikat
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Telangana
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Hyderabad, Telangana, Intia, 500032
- AIG Hospitals
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Ottaa yhteyttä:
- Aig research, MD, DM
- Puhelinnumero: 09182645727
- Sähköposti: aigresearch7@gmail.com
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Päätutkija:
- Dr. Sundeep Lakhtakia, MD, DM
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Alatutkija:
- Dr. Anudeep Katrevula, MD, DM
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Alatutkija:
- Dr. Jahangeer Basha, MD, DM
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Osallistumiskriteerit
Kelpoisuusvaatimukset
Opintokelpoiset iät
- Aikuinen
- Vanhempi Aikuinen
Hyväksyy terveitä vapaaehtoisia
Näytteenottomenetelmä
Tutkimusväestö
Kuvaus
Inclusion Criteria:
- Adults aged 18 years or older.
- Undergoing clinically indicated diagnostic endoscopic ultrasound (EUS).
- Same-day FibroScan examination available.
- Controlled Attenuation Parameter (CAP) <238 dB/m.
- Liver Stiffness Measurement (LSM) <7.5 kPa.
- At least 10 valid FibroScan measurements.
- FibroScan interquartile range (IQR)/median ≤30%.
- Able and willing to provide written informed consent.
Exclusion Criteria:
- Known chronic liver disease.
- Hepatitis B or Hepatitis C infection.
- Significant alcohol consumption.
- Decompensated cirrhosis.
- Portal vein thrombosis.
- Ascites.
- Focal liver lesion.
- Previous liver surgery.
- Pregnancy.
- Inadequate FibroScan examination.
- Poor-quality EUS-guided Attenuation Imaging (ATI) or Shear Wave Elastography (SWE) acquisition.
- Incomplete study data or withdrawal of informed consent.
Opintosuunnitelma
Miten tutkimus on suunniteltu?
Suunnittelun yksityiskohdat
Kohortit ja interventiot
Ryhmä/Kohortti |
Interventio / Hoito |
|---|---|
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Normal FibroScan Cohort
Adults aged 18 years or older undergoing clinically indicated diagnostic endoscopic ultrasound (EUS) for non-hepatobiliary indications who have normal FibroScan findings (Controlled Attenuation Parameter [CAP] <238 dB/m and Liver Stiffness Measurement [LSM] <7.5 kPa).
Participants will undergo EUS-guided Attenuation Imaging (ATI) and Shear Wave Elastography (SWE) of the right and left hepatic lobes during the same EUS procedure to establish preliminary reference values and assess the feasibility and reliability of these quantitative imaging techniques.
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A clinically indicated diagnostic endoscopic ultrasound will be performed according to standard institutional practice.
During the examination, the liver will be visualized from the stomach and duodenum to allow quantitative liver assessment.
Attenuation Imaging (ATI) will be performed during the diagnostic EUS to quantitatively assess hepatic steatosis.
Five valid ATI measurements will be obtained from both the right and left hepatic lobes under direct EUS visualization.
Measurements meeting predefined quality criteria will be used for analysis.
Shear Wave Elastography (SWE) will be performed during the diagnostic EUS to assess liver stiffness.
Ten valid measurements will be obtained from both the right and left hepatic lobes.
Shear wave velocity (m/s) and tissue elasticity (kPa) will be recorded, and only measurements meeting predefined quality criteria will be included in the analysis.
Participants will undergo same-day FibroScan examination before EUS to confirm normal liver stiffness and steatosis.
Controlled Attenuation Parameter (CAP) and Liver Stiffness Measurement (LSM) will be recorded, with at least 10 valid measurements and acceptable quality metrics required for study eligibility.
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Mitä tutkimuksessa mitataan?
Ensisijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
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Reference values for EUS-guided Attenuation Imaging (ATI)
Aikaikkuna: During the index EUS procedure (Day 0)
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To establish preliminary reference values for EUS-guided Attenuation Imaging (ATI) in the right and left hepatic lobes of adults with normal FibroScan findings.
ATI values will be reported as mean ± standard deviation (SD), median (interquartile range [IQR]), and 95% reference intervals.
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During the index EUS procedure (Day 0)
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Reference values for EUS-guided Shear Wave Elastography (SWE) elasticity
Aikaikkuna: During the index EUS procedure (Day 0)
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To establish preliminary reference values for EUS-guided SWE elasticity (kPa) in the right and left hepatic lobes.
Results will be reported as mean ± SD, median (IQR), and 95% reference intervals.
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During the index EUS procedure (Day 0)
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Reference values for EUS-guided Shear Wave Elastography (SWE) velocity
Aikaikkuna: During the index EUS procedure (Day 0)
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To establish preliminary reference values for EUS-guided SWE shear wave velocity (m/s) in the right and left hepatic lobes.
Results will be reported as mean ± SD, median (IQR), and 95% reference intervals.
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During the index EUS procedure (Day 0)
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Toissijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
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Technical success rate
Aikaikkuna: During the index EUS procedure (Day 0)
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To determine the proportion of participants in whom acceptable EUS-guided ATI and SWE measurements are successfully acquired according to predefined quality criteria.
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During the index EUS procedure (Day 0)
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Measurement reliability
Aikaikkuna: During the index EUS procedure (Day 0)
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To evaluate the reliability and reproducibility of EUS-guided ATI and SWE measurements using predefined quality parameters.
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During the index EUS procedure (Day 0)
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Agreement between right and left hepatic lobe measurements
Aikaikkuna: During the index EUS procedure (Day 0)
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To assess agreement between ATI and SWE measurements obtained from the right and left hepatic lobes.
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During the index EUS procedure (Day 0)
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Correlation between ATI and FibroScan CAP
Aikaikkuna: During the index EUS procedure (Day 0)
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To evaluate the correlation between EUS-guided ATI measurements and FibroScan Controlled Attenuation Parameter (CAP).
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During the index EUS procedure (Day 0)
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Correlation between SWE and FibroScan Liver Stiffness Measurement (LSM)
Aikaikkuna: During the index EUS procedure (Day 0)
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To evaluate the correlation between EUS-guided SWE measurements and FibroScan Liver Stiffness Measurement (LSM).
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During the index EUS procedure (Day 0)
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Acquisition time
Aikaikkuna: During the index EUS procedure (Day 0)
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To determine the time required to complete EUS-guided ATI and SWE measurements during the diagnostic EUS examination.
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During the index EUS procedure (Day 0)
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Yhteistyökumppanit ja tutkijat
Opintojen ennätyspäivät
Opi tärkeimmät päivämäärät
Opiskelun aloitus (Arvioitu)
Ensisijainen valmistuminen (Arvioitu)
Opintojen valmistuminen (Arvioitu)
Opintoihin ilmoittautumispäivät
Ensimmäinen lähetetty
Ensimmäinen toimitettu, joka täytti QC-kriteerit
Ensimmäinen Lähetetty (Todellinen)
Tutkimustietojen päivitykset
Viimeisin päivitys julkaistu (Todellinen)
Viimeisin lähetetty päivitys, joka täytti QC-kriteerit
Viimeksi vahvistettu
Lisää tietoa
Tähän tutkimukseen liittyvät termit
Avainsanat
Muita asiaankuuluvia MeSH-ehtoja
- Patologiset prosessit
- Ruoansulatuskanavan sairaudet
- Maksasairaudet
- Fibroosi
- Patologiset tilat, merkit ja oireet
- Maksakirroosi
- Tutkintatekniikat
- Näytteenkäsittely
- Kliiniset laboratoriotekniikat
- Diagnostiikkatekniikat ja menettelyt
- Diagnoosi
- Kirurgiset toimenpiteet, operatiivinen
- Minimaalisesti invasiiviset kirurgiset toimenpiteet
- Sytologiset tekniikat
- Biopsia
- Sytodiagnoosi
- Diagnostiikkatekniikat, kirurginen
- Diagnostinen kuvantaminen
- Ultraääni
- Biopsia, hieno neula
- Biopsia, neula
- Kuvaohjattu biopsia
- Ultraääni, interventio
- Endoskooppinen ultraääniohjattu hieno neulan aspiraatio
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