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NCT05651724Recruiting

Global Research Initiative for Patients Screening on MASH

Global Research Initiative for Patients Screening on MASH - Implementation of an International Transmural Patient Care Pathway

Source: ClinicalTrials.gov · Last updated 1 Aug 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Observational
Enrollment
10000 (estimated)
First submitted
18 Oct 2022
Start date
30 Jun 2023
Primary completion date
31 Mar 2031
Lead sponsor
Julius Clinical
NCT number
NCT05651724

What you commit to

  • Study type: Observational
  • Planned participants: 10000
  • From 30 Jun 2023 to the primary completion date, 31 Mar 2031
  • 13 sites in 10 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • The patient underwent bariatric surgery in the last 12 months.

Other illness

  • 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 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;

Other

  • 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 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.

Who the study is looking for

  • 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)

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (13)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Antwerp University Hospital
Coordinator of this site? Confirm its status
AntwerpBelgiumActive, not recruiting
Hôpital Erasme - Cliniques universitaires de Bruxelles
Coordinator of this site? Confirm its status
BrusselsBelgiumRecruiting
4th internal clinic General University Hospital
Coordinator of this site? Confirm its status
PragueCzechiaNot yet recruiting
Universitätsklinikum des Saarlandes
Coordinator of this site? Confirm its status
HomburgGermanyNot yet recruiting
Universitätsmedizin Mainz
Coordinator of this site? Confirm its status
MainzGermanyRecruiting
Hospital Universitario Virgen del Rocio
Coordinator of this site? Confirm its status
SevilleSpainRecruiting
Hôpital de la Pitié-Salpêtrière
Coordinator of this site? Confirm its status
ParisFranceNot yet recruiting
Harokopio University of Athens
Coordinator of this site? Confirm its status
AthensGreeceNot yet recruiting
Fondazione Policlinico Universitario Agostino Gemelli IRCCS (FPG), Università Cattolica del Sacro Cuore (UCSC)
Coordinator of this site? Confirm its status
RomeItalyNot yet recruiting
Amsterdam UMC
Coordinator of this site? Confirm its status
AmsterdamNetherlandsRecruiting
Franciscus Gasthuis & Vlietland
Coordinator of this site? Confirm its status
RotterdamNetherlandsRecruiting
ULSSM - Unidade Local de Saúde Santa Maria, E.P.E
Coordinator of this site? Confirm its status
LisbonPortugalRecruiting
Sacele Municipal Hospital
Coordinator of this site? Confirm its status
SăceleRomaniaNot yet recruiting

This page is information, not medical advice. Discuss any trial with your doctor.