Clinical trial Recruiting at 1 site Observational Ages 18 and up

Global Reference Ranges for Healthy Adults in Singapore

Official title: Global Reference Ranges - Singapore

Run by Perspectum · NCT07166471 · Data updated 2026-11-12

This study tests healthy adults in Singapore to establish normal MRI-based reference values for liver and body measurements and to see if these ranges differ by ethnicity.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment50 (estimated)
SponsorPerspectum
Industry-sponsored
Locations1 site (Singapore)
StatusRecruiting
StartedJanuary 1, 2026
Main results expectedSeptember 2027
Study endsSeptember 2027
Registry record updatedJuly 15, 2026
Trial IDNCT07166471 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Healthy adults 18 years or older who can undergo MRI and consent to participate, with no active cardiovascular disease or major organ-related conditions.

Probably not a fit

Individuals with cardiovascular or significant systemic health issues or MRI contraindications may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The Global Reference Range Study (GRR) collects MRI data from self-reported healthy adults to generate reference values for fibroinflammation, fat, organ sizes, and other abdominal and thoracic measurements. It aims to determine ethnicity-specific reference ranges when applicable. Enrollment requires adults 18+, willing to consent, and eligible for MRI with no major cardiovascular or organ-related contraindications. The study is observational and led by Perspectum with the National Heart Centre Singapore as a collaborator at a Singapore site.

Why it matters

Potential benefit: If successful, the results could better define normal ranges for imaging-based health assessments and improve interpretation across diverse populations.

How similar studies have gone: Previous imaging-reference studies have demonstrated feasibility in establishing population-specific reference ranges, supporting the potential value of this approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Male or female at least 18 years of age
* Self-reported healthy
* Willing and able to give informed consent for participation in the study
* Willing and able to undergo an MRI

Exclusion Criteria:

* History of cardiovascular disease as follows:

  * Myocardial infarction
  * Heart failure
  * Cardiomyopathy
  * Stroke
  * Hospital admission/discharge for unstable angina
  * Heart surgery
  * Unstable angina
  * Transient ischemic attack
* Presence of CVD risk factors such as hypertension, hyperlipidaemia, Type 2 diabetes, BMI \> 30 kg/m2, smoker (current/ex-smoker)
* History of non-cardiac diseases related to the lungs, liver, kidneys, pancreas or spleen judged by the study investigator as therefore unsuitable to participate in the study
* The participant may not enter the study if they have any contraindication to magnetic resonance imaging (standard MRI exclusion criteria including pregnancy, extensive tattoos, pacemaker, shrapnel injury, severe claustrophobia)
* Any other cause, including a significant disease or disorder which, in the opinion of the investigator, may either put the participant at risk because of participation in the study, or may influence the participant's ability to participate in the study

Where it's running

  • National Heart Centre Singapore
    Singapore, Singapore
    Recruiting

Study contacts

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
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Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.