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

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorM.D. Anderson Cancer Center

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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.

Hereditary cancer syndromes or known pathogenic germline mutations associated with pancreatic cancer risk

Family history of pancreatic ductal adenocarcinoma (PDAC)

Disqualifiers

BMI < 18.5 Kg/m2

Documented history of symptomatic hypoglycemia

Pregnant or breastfeeding women

Cognitively impaired individuals

Trial design

Design model

Single group

Treatments tested in this trial

  • intermittent fasting

    Other intervention

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

Treatment groups

20 Participants
are divided into 1 treatment group
Group A: Intermittent fastingExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Safety and adverse events (AEs).

Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 5.0

Time frame
Through study completion; an average of 1 year.

Secondary outcomes

Other outcomes

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: