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Blood sugar control may boost chemo in pancreatic cancer

NCT ID NCT05132244

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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

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

About 50 people

The number the study aims to enrol. It can still change while the study runs.

Started

Apr 2024

Expected to finish

Oct 2028

An estimate. End dates often move.

Lead sponsor

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

18 years and older

Sex

Anyone

Healthy volunteers

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

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.

  1. The places running it

    2 sites. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. 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

  • British Columbia Cancer

    RECRUITING

    Vancouver, British Columbia, V5Z 4E6, Canada

  • Princess Margaret Cancer Centre

    RECRUITING

    Toronto, Ontario, M5G 2M9, Canada

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