Status:

TERMINATED

New Onset Diabetes Management for Earlier Detection of Pancreatic Cancer (NODMED)

Lead Sponsor:

ClearNote Health

Conditions:

Pancreatic Cancer

Eligibility:

All Genders

50+ years

Phase:

NA

Brief Summary

Bluestar Genomics has developed a non-invasive test that aids in detection of occult pancreatic cancer in patients with new onset type II diabetes (NOD) who are 50 years old or older. The purpose of t...

Detailed Description

This is a prospective longitudinal and interventional study of the Bluestar Genomics early detection pancreatic cancer test. The test will be ordered and results returned to site-investigators. The st...

Eligibility Criteria

Inclusion

  • ≥ 50 years of age or older at the time of enrollment
  • Willing to sign the informed consent form
  • Must have 2 occurrences from among the below parameters of diabetes mellitus (PDMs) in past 90 days measured in outpatient setting (not in urgent care, emergency room or while inpatient):
  • FBG ≥126mg/dl HbA1c ≥6.5% RBG ≥ 200mg/dl 2-hour post-glucose ≥200mg/dl (OGTT)
  • Must have had glycemic parameter measured in 3-18 months prior to screening that did NOT meet DM criteria
  • Must be willing to provide several tubes of blood without endangering health
  • No history of pancreatic cancer or other known pancreatic neoplasia
  • No active cancers within the past 5 years (with the exception of non-melanoma skin cancers resolved/treated \> 1 year prior to enrollment and in situ cancers)

Exclusion

  • Prior DM diagnosis
  • Met criteria for DM ≥91 days prior to enrollment (patients with prior gestational diabetes that has resolved are NOT acceptable to enroll)
  • Carried a DM diagnosis or used anti-DM medications at a time greater than or equal to 91 days prior to enrollment
  • Any known pancreatic lesions (aside from diabetes)
  • Received cancer treatment within the past 5 years (with the exception of treatment of non-melanoma skin cancer), carrying a current cancer diagnosis, and/or being investigated for suspicion of past cancer recurrence.
  • Current chronic or acute oral steroid use
  • History of intra-articular steroid injections (\<1 week) of the qualifying DM blood test (allowed exception: nasal, topical, oral budesonide)
  • Any surgery requiring general anesthesia within 2 months of collection
  • Local anesthetic (including dental novocaine) within 1 week of collection
  • History or presence of HIV/AIDs, Hepatitis A or E within the past five years, TB, any kind of prion disorder (e.g., CJD)
  • Blood transfusion within 1 month
  • Organ transplant recipient
  • Currently pregnant, or pregnancy within last 12 months
  • Receipt of systemic immunomodulation therapy within past 12 months
  • Significant medical condition that in the site investigator's opinion would compromise the subject's ability to tolerate study interventions

Key Trial Info

Start Date :

October 31 2022

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

March 16 2023

Estimated Enrollment :

26 Patients enrolled

Trial Details

Trial ID

NCT05188586

Start Date

October 31 2022

End Date

March 16 2023

Last Update

September 19 2024

Active Locations (5)

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Page 1 of 2 (5 locations)

1

Headlands Research - Scottsdale - PPDS

Scottsdale, Arizona, United States, 85260-6411

2

JEM Research Institute - Headlands - PPDS

Atlantis, Florida, United States, 33462-6631

3

Prisma Health/Endocrinology specialist and Thyroid

Greenville, South Carolina, United States, 29605-4289

4

Consano Clinical Research, LLC

Shavano Park, Texas, United States, 78231-1281