Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Understanding pancreatic fat and cyst features in patients

Official title: Determination of Pancreatic Steatosis Prevalence and Correlation With High-risk Cyst Features in Patients With Pre-malignant Pancreatic Cystic Neoplasms Using Magnetic Resonance Imaging and Endoscopic Ultrasound

Run by Chinese University of Hong Kong · NCT05334836 · Data updated 2026-11-12

This study is trying to see if measuring fat in the pancreas and liver can help find early signs of dangerous pancreatic cysts in patients who might be at risk for pancreatic cancer.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment236 (estimated)
SponsorChinese University of Hong Kong
Academic / other
Drugs / interventionsradiation
Locations1 site (Shatin, New Territories)
StatusRecruiting
StartedApril 6, 2022
Main results expectedApril 30, 2027
Study endsApril 30, 2027
Registry record updatedOctober 27, 2026
Trial IDNCT05334836 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include adults aged 18 or older with at least one pancreatic cystic lesion or healthy subjects.

Probably not a fit

Patients with known pancreatic cancer, prior pancreatic resection, or significant alcohol consumption 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

This study aims to determine the prevalence of pancreatic steatosis and its correlation with high-risk features of pancreatic cysts. It involves screening patients with pancreatic cystic lesions presumed to be intraductal papillary mucinous neoplasms (IPMN) or mucinous cystic neoplasms (MCN) using MRI for quantifying pancreatic and liver fat. The goal is to enhance early detection and surveillance of pre-malignant lesions to improve outcomes for patients at risk of pancreatic cancer.

Why it matters

Potential benefit: If successful, this study could lead to earlier detection and better management of pancreatic cancer, potentially improving survival rates.

How similar studies have gone: Other studies have shown promise in using imaging techniques for early detection of pancreatic lesions, indicating that this approach may be beneficial.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Age 18 or older
2. Patients with at least 1 pancreatic cystic lesion presumed to be IPMN or MCN based on CT, MRI or EUS features, with a cyst size ≥ 5mm; or healthy subjects.
3. Patients who are able to provide written informed consent to participate in the study and comply with the study procedures.

Exclusion Criteria:

1. Unable to provide written informed consent
2. Patients with metallic implants or other contraindications to MRI
3. Patients with contraindications for endoscopy due to comorbidities
4. Patients with known pancreatic cancer or prior pancreatic resection
5. Patients with significant alcohol consumption, defined as alcohol intake of over 20 g daily (140 g weekly) for men and 10 g daily (70 g weekly) for women

Where it's running

  • Prince of Wales Hospital, The Chinese University of Hong Kong
    Shatin, New Territories, Hong Kong
    Recruiting

Study contacts

  • Principal investigator: Raymond S Tang, MD — Chinese University of Hong Kong
  • Study coordinator: Felix Sia
  • Email: felixsia@cuhk.edu.hk
  • Phone: 26370428

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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.
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.