๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-02-10

Diabetes RElated to Acute Pancreatitis and Its Mechanisms: Metabolic Outcomes Using Novel CGM Metrics (NCT06401577)

Diabetes RElated to Acute Pancreatitis and Its Mechanisms: Metabolic Outcomes Using Novel CGM Metrics (DREAM-ON) - An Observational Cohort Study From the Type 1 Diabetes in Acute Pancreatitis Consortium (T1DAPC)

๐ŸŸข Recruiting Interventional Protocol ๐Ÿ“Š Observational Clinical Research Sponsor: Milton S. Hershey Medical Center

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

The DREAM-ON study will investigate whether continuous glucose monitoring (CGM) is useful to predict risk for developing diabetes mellitus (DM) and pre-diabetes mellitus (PDM), the need for insulin therapy among those who develop DM, and to determine whether CGM can provide insight into the pathophysiology and DM subtype among participants who have experienced an episode of acute pancreatitis (AP). Thus, the results of the DREAM-ON study could inform future clinical practice guidelines for the management AP as well as potentially extending the licensing authorization for CGM to include use in patients with pancreatogenic (Type 3c) DM.

Who can join: Review the eligibility criteria below.

Location: University of Southern California โ€” Los Angeles, California

Age range: 18 Years to 75 Years

๐Ÿงช Interventions in This Study

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria โ†—

๐Ÿ“ All Participating Trial Locations (13 Sites)

  • University of Southern California โ€” Los Angeles, California
  • Cedars-Sinai Medical Center โ€” Los Angeles, California
  • Stanford University โ€” Stanford, California
  • University of Florida โ€” Gainesville, Florida
  • AdventHealth โ€” Orlando, Florida
  • Northwestern University โ€” Chicago, Illinois
  • University of Illinois at Chicago โ€” Chicago, Illinois
  • Indiana University โ€” Indianapolis, Indiana
  • Johns Hopkins University โ€” Baltimore, Maryland
  • University of Minnesota โ€” Minneapolis, Minnesota
  • Ohio State University โ€” Columbus, Ohio
  • University of Pittsburgh โ€” Pittsburgh, Pennsylvania
  • Benaroya Research Institute โ€” Seattle, Washington

๐Ÿ“ž Contact the Study Coordinator

Phone: (717) 531-3851

Email: rzimmerman1@pennstatehealth.psu.edu

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

๐Ÿ’ฐ Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

๐Ÿ’ก How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
๐Ÿ›๏ธ View Official NIH Record โ†—