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Identify microRNAs in Cachexia in Pancreatic Carcinoma

Pilot Trial to Identify microRNAs in Cachexia in Patients With Pancreatic Carcinoma

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05275075
Acronym
SCC-miRPanCa
Enrollment
40
Registered
2022-03-11
Start date
2022-12-07
Completion date
2026-04-03
Last updated
2026-06-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Resectable Pancreatic Adenocarcinoma

Keywords

pancreatic cancer, cachexia, microRNA, mRNA, PDAC

Brief summary

The purpose of this study is to determine the proportion of pancreatic patients who experience weight loss and cachexia, and to identify any differences in the genes between patient groups.

Detailed description

This research study will retrospectively examine 1395 patients from the University of Alabama and the University of Oklahoma Stephenson Cancer Center (OU-SCC) pancreatic cancer cohorts. The prospective arm, will enroll a total of 100 eligible volunteers at the OU-SCC. The demographic and medical data from the retrospective and prospective arms will be combined (1495 patients) to ascertain any racial disparities in pancreatic cancer patients with cachexia. Perspective volunteers at the OU-SCC will undergo routine tests to determine if their cancer is operable. Pancreatic tumors will be removed from the eligible patients, as part of their normal standard of care and will be examined for genes that may be related to unexplained muscle loss and compared to tumor tissue from other patients with pancreatic cancer. An optional hand strength exam, and standing on a scale that measures weight, muscle, and body fat will be available to OU-SCC patients.

Interventions

OTHERPancreatic cancer microRNA and messenger RNA expression.

Tumor specimens from pancreatic patients will be analyzed for markers associated with muscle loss.

Sponsors

University of Oklahoma
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Male or female patient, who is ≥ 18 years old at the time of informed consent. 2. Patients with operable pancreatic tumors diagnosed in the last 12 months prior to consent with clinical discretion or pathology confirmed as adenocarcinoma. 3. Patient has stage I or higher disease who is considered a candidate for surgical resection of pancreatic cancer, with or without neoadjuvant chemotherapy. 4. Ability to provide written informed consent and HIPAA authorization.

Exclusion criteria

1. Patients with pancreatic adenocarcinoma who do not meet the criteria for surgical resection. 2. Patient has cancer diagnosis other than primary pancreatic adenocarcinoma.

Design outcomes

Primary

MeasureTime frameDescription
Proportion of African American pancreatic cancer patients with weight loss and cachexia.1 - 12 monthsEvaluate weight loss and the markers of cachexia, albumin and psoas cross-sectional area, to see if African Americans with pancreatic cancer patients experience Grade I-IV cachexia at a higher frequency than other racial groups.

Secondary

MeasureTime frameDescription
Differences in microRNA and messenger RNA tumor expression profiles in all cancer patients undergoing pancreatic surgery.1 - 12 monthsAssess fold-change expression differences in microRNA and messenger RNA tumor expression profiles in all cancer patients undergoing pancreatic surgery.
Differences in cachexia-associated RNA signatures in African American pancreatic cancer patients, and other racial groups.1 - 12 monthsAssess fold-change expression differences in cachexia-associated RNA signatures in African American pancreatic cancer patients, and other racial groups.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORAjay Jain, MD

University of Oklahoma Stephenson Cancer Center

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 2, 2026