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 type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 50 (estimated) |
| Sponsor | Perspectum Industry-sponsored |
| Locations | 1 site (Singapore) |
| Status | Recruiting |
| Started | January 1, 2026 |
| Main results expected | September 2027 |
| Study ends | September 2027 |
| Registry record updated | July 15, 2026 |
| Trial ID | NCT07166471 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
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National Heart Centre Singapore
Singapore, Singapore Recruiting
Study contacts
- Study coordinator: Masliza Mahmod
- Email: masliza.mahmod@perspectum.com
- Phone: 001865655343
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.