Blood sugar control may boost chemo in pancreatic cancer
NCT ID NCT05132244
First seen Jun 26, 2026 · Last updated Sep 15, 2026 · Updated 2 times
Summary
This pilot study looks at whether closely monitoring and managing blood sugar levels can help people with pancreatic cancer. About 50 participants will wear a continuous glucose monitor during chemotherapy. Half will get intensive glucose management from an endocrinologist, while the other half gets standard care. The goal is to see if tight glucose control is feasible and might improve cancer outcomes.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- standard anti-hyperglycemic drugs (metformin, insulin, GLP-1 agonists, SGLT2 inhibitors, DPP-4 inhibitors)
- What this could lead to
- If it works, this could show that tight glucose control improves how well chemotherapy works for pancreatic cancer.
- What could go wrong
- This is a small pilot study with only 50 people, so results may not apply to everyone. It is testing feasibility, not yet proving benefit.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 50 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Apr 2024
- Expected to finish
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Oct 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Histological/cytological diagnosis of pancreatic ductal adenocarcinoma (PDAC). * Planned to undergo first-line systemic therapy. * Age greater than or equal to 18 years. * Eastern Cooperative Oncology Group (ECOG) performance status 0-1. * Adequate bone marrow and organ function as defined by the following laboratory values: 1. Absolute neutrophil count (ANC) greater than or equal to 1.5 x 10\^9/L. 2. Platelet count greater than or equal to 75 x 10\^9/L. 3. Hemoglobin greater than or equal to 9.0 g/dL. 4. Estimated glomerular filtration rate (GFR) by Cockroft-Gault equation OR 24 hour urine collection greater than or equal to 40 ml/min. 5. Creatinine clearance greater than or equal to 40 mL/min using Cockcroft-Gault formula. 6. Potassium within normal limits, or corrected with supplements. 7. International normalized ratio (INR) less than or equal to 1.5. 8. Total serum bilirubin less than or equal to 2 x upper limit of normal (ULN) (any elevated bilirubin should be asymptomatic at enrollment) except for participants with documented Gilbert's syndrome who may only be included if the total bilirubin less than or equal to 3 x ULN or direct bilirubin less than or equal to 1.5 x ULN). 9. Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) less than or equal to 2.5 x ULN (or less than or equal to 5 x ULN if liver metastases are present). * Able to understand and voluntarily sign the informed consent form. * Able to comply with the study visit schedule and other protocol requirements. * Able to swallow oral medications. * Measurable or evaluable disease by Response Evaluation Criteria in Solid Tumours (RECIST) 1.1 at baseline. * Life expectancy of more than 90 days as judged by the study doctor. Exclusion Criteria: * Absence of distant or lymph node metastases. Participants with borderline resectable or locally advanced PDAC are not eligible. * Received prior systemic therapy (chemotherapy or any other anti-cancer agent) for treatment of metastatic PDAC. Participants who received adjuvant chemotherapy after surgical resection of early stage disease are eligible. * Currently receiving anti-cancer therapy (chemotherapy or any other anti-cancer agent). * Presence of brain metastases. * Known diagnosis of type I diabetes where strict glucose control and close Endocrinology follow-up is already indicated. * Known diagnosis of type II diabetes and already followed by Endocrinologist. * Participants with a positive pregnancy test. * Participants who are not safe to include in the study as judged by the study doctor for any medical or non-medical reason. * Unable to comply with study assessments and follow-up.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
2 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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British Columbia Cancer
RECRUITINGVancouver, British Columbia, V5Z 4E6, Canada
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Princess Margaret Cancer Centre
RECRUITINGToronto, Ontario, M5G 2M9, Canada
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