Trial0

Clinical trial · NCT07513116 · NOT_YET_RECRUITING · NA

Evaluating Intermittent Fasting In Individuals At High Risk ForPancreatic Cancer Undergoing Screening

Sponsor: M.D. Anderson Cancer Center

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Summary

To learn whether an eating pattern called intermittent fasting (IF) is tolerable and feasible for individuals at high risk of pancreatic cancer and whether IF is associated with changes in biological markers, including metabolic, inflammatory, microbiome, and imaging-related markers.

Interventions

  • intermittent fasting · OTHER

    They will fast for 16 consecutive hours each day and have an 8-hour window for eating.

Published eligibility criteria

Verbatim from the registry. Only the site can decide how these apply to a specific patient.

Inclusion Criteria

* Participants ≥ 18 years old. Participants under 18 are excluded due to their potential inability to understand and consent independently to the methods required for the study drug use and its potential risks and benefits.
* Participants evaluated and classified as high risk for pancreatic cancer through a High-Risk Pancreatic Cancer Clinic or High-Risk Pancreatic Cyst Clinic, based on established clinical assessment and risk stratification.
* High-risk status may include one or more of the following:

  * Hereditary cancer syndromes or known pathogenic germline mutations associated with pancreatic cancer risk
  * Family history of pancreatic ductal adenocarcinoma (PDAC)
  * Presence of pancreatic cysts or precursor lesions (e.g., IPMN, MCN)
  * New-onset diabetes mellitus is considered suspicious for pancreatic cancer
  * History of recurrent or chronic pancreatitis
* Eligibility and surveillance risk assessment must be consistent with NCCN (National Comprehensive Cancer Network) Guidelines for Pancreatic Cancer Screening in High- Risk Individuals.
* Participants are able to understand and are willing to sign a written informed consent document.
* Both English-speaking and non-English-speaking participants are eligible for participation
* Participants are willing to make a change in eating time patterns.
* Participants are willing to provide App-tracked fasting time data over the course of the study.

Exclusion Criteria

* BMI \< 18.5 Kg/m2
* Documented history of symptomatic hypoglycemia
* Pregnant or breastfeeding women
* Cognitively impaired individuals

Sites (1)

  • MD Anderson Cancer Center, Houston, Texas

Not medical advice. Trial0 is a navigation service, not a medical provider. Nothing here is medical advice or a recommendation to pursue any treatment; eligibility matching is informational, based on published registry criteria, and only the trial site or treating clinician can determine actual eligibility. Decisions belong with the patient and their own doctors. Registry data refreshed at most hourly; last update posted 2026-04-14.