Clinical Trials in Germany / NCT05651724
Recruiting Observational

Global Research Initiative for Patients Screening on MASH

NCT05651724 · tracked via the Priya Life Science Germany tracker
Sponsor
Julius Clinical
Phase
Observational
Started
2023-06-30
Last updated
2024-08-01

Condition(s) studied

MASHMASLDMASH With FibrosisFibrosis, LiverSteatosis of LiverType 2 DiabetesObesityMetabolic SyndromeArterial Hypertension

Study summary

GRIPonMASH will assist (primary) health care providers clinicians to implement the latest patient care pathway, as described by the European Association for the Study of the Liver (EASL), to identify patients at risk of severe metabolic dysfunction-associated steatotic liver disease (MASLD) and to raise awareness. The primary objective is to implement a transmural patient care pathway, in order to identify patients with MASLD and its progressive form metabolic dysfunction-associated steatohepatitis (MASH) in primary care centres and clinics in 10 European countries.

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: * Newly diagnosed subjects should fulfil criteria for diagnosis of type 2 diabetes mellitus or metabolic syndrome or obesity or arterial hypertension, following the study definitions. * Subjects that are currently being treated for type 2 diabetes mellitus or metabolic syndrome or obesity or arterial hypertension, should have had a prior diagnosis based on study definitions. Study definitions: Type 2 diabetes mellitus * At least 2 times a fasting glucose \> 7,0 mmol/L * Or elevated non-fasting glucose \>11,1 mmol/L 2 hrs after OGTT * Or HbA1c ≥48 mmol/mol (≥6.5%) * Or being actively treated for previously diagnosed type 2 diabetes by a health care provider Obesity * Body mass index (BMI) \> 30 * Or waist circumferences Caucasian: male ≥ 94 cm, female ≥ 80 cm South-Asian/Chinese: male ≥90 cm, female ≥80 cm Japanese: male ≥85 cm, female ≥90 cm Arterial hypertension * Systolic BP ≥ 140 mmHg and/or diastolic BP ≥ 90 mmHg * Or being actively treated for previously diagnosed arterial hypertension by a health care provider Metabolic syndrome \- Central obesity defined as waist circumference (see above), if BMI is \>30 kg/m2, central obesity can be assumed and waist circumference does not need to be measured AND any two of the following: * Raised triglycerides: ≥ 150 mg/dL (1.7 mmol/L), or specific treatment for this lipid abnormality * Reduced HDL cholesterol: \< 40 mg/dL (1.03 mmol/L) in males, \< 50 mg/dL (1.29 mmol/L) in females, or specific treatment for this lipid abnormality * Raised blood pressure (BP): systolic BP ≥ 130 or diastolic BP ≥ 85 mm Hg, or treatment of previously diagnosed hypertension * Raised fasting plasma glucose (FPG): FGP ≥ 100 mg/dL (5.6 mmol/L), or previously diagnosed type 2 diabetes (if above \>5.6 mmol/L or 100 mg/dL, an oral glucose tolerance test is strongly recommended, but is not necessary to define presence of the syndrome) Exclusion Criteria: * The patient is known with hepatitis B, C or HIV or any other liver condition (like hemochromatosis, sarcoidosis, Wilson's disease etc); * The patient is known with any other condition that may lead to liver fibrosis or cirrhosis; * The patient engages in (excessive) alcohol use: \> 3 units/day in males \[30 grams/day\] and \> 2 units/day in females \[20 grams/day\]; * The patient has a history or evidence of any other clinically significant condition or planned or expected procedure that in the opinion of the Investigator, may compromise the patient's safety or ability to be included in this study; * The patient is an employee or contractor of the facility that is conducting the study or is a family member of the Investigator, sub-Investigator, or any Sponsor personnel; * The patient is not able to understand the details of the protocol and/or is not able to provide written informed consent; * The patient is pregnant or breastfeeding. * The patient underwent bariatric surgery in the last 12 months.

Primary outcome measure(s)

Trial sites (13)

FacilityCityRegionStatus
Hôpital Erasme, Cliniques Universitaires De Bruxelles Brussels Vlaams-brabant Recruiting
Antwerp University Hospital Antwerp Belgium Active Not Recruiting
4th internal clinic General University Hospital Prague Bohemia Not Yet Recruiting
Hôpital de la Pitié Salpêtrière Paris Il-de-France Not Yet Recruiting
Universitätsmedizin Mainz Mainz Rhineland-Palatinate Recruiting
Universitätsklinikum des Saarlandes Homburg Saarland Not Yet Recruiting
Harokopio University of Athens Athens Greece Not Yet Recruiting
Fondazione Policlinico Universitario Agostino Gemelli IRCCS (FPG), Università Cattolica del Sacro Cuore (UCSC) Rome Lazio Not Yet Recruiting
Amsterdam UMC Amsterdam South Holland Recruiting
Franciscus Gasthuis & Vlietland Rotterdam South Holland Recruiting
ULSSM - Unidade Local de Saúde Santa Maria, E.P.E Lisbon Portugal Recruiting
Sacele Municipal Hospital Săcele Brașov County Not Yet Recruiting
Hospital Universitario Virgen del Rocío Seville Spain Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05651724 on ClinicalTrials.gov ↗ ← All trials in Germany