Glycemic Impact on Glioblastoma Outcomes

Sponsor
University Health Network, Toronto (Other)
Overall Status
Withdrawn
CT.gov ID
NCT03235934
Collaborator
Sinai Health System (Other)
0
1
13.8
0

Study Details

Study Description

Brief Summary

This pilot study aims to evaluate the feasibility of close glucose monitoring and management of patients (targeting fasting and pre-meal glucose of 4-7 mmol/L) using state-of-the-art flash glucose monitoring (FGM) technology. The glycemic intervention will be personalized based on individual blood glucose levels. Although the glycemic interventions used in this study include standard medications and methods of glucose monitoring used for patients with diabetes, this pilot study will specifically evaluate the feasibility of using these approaches in patients with GBM, appreciating their additional medical, functional and social challenges.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The purpose of this pilot study is to determine the feasibility of using close monitoring and management of glucose levels in patients undergoing radiation and chemotherapy for glioblastoma.

    The glucose management will include the use of standard metformin a common treatment for patients with early type 2 diabetes that has also shown anti-tumor effects in GBM, and will be further personalized based on individual blood glucose levels. Additional anti-hyperglycemic management will be provided at the discretion of the Endocrinologist.

    Close glucose monitoring will include flash glucose monitoring (FGM) with a device called an FreeStyle Libre Pro Flash Glucose Monitoring System, finger-prick glucose measures (standard approach for patients with diabetes) and weekly blood tests (our current standard for patients with GBM).

    In addition to determining the feasibility of using these approaches, this pilot study will help identify the simplest and most effective approach of managing glucose levels in patients with GBM appreciating their additional medical, functional and social challenges.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    0 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Glycemic Impact on Glioblastoma Outcomes
    Anticipated Study Start Date :
    Dec 1, 2018
    Anticipated Primary Completion Date :
    Oct 1, 2019
    Actual Study Completion Date :
    Jan 24, 2020

    Outcome Measures

    Primary Outcome Measures

    1. Total time spent in target glucose level [1 week]

      total time spent in target range of 4-10 mmol/L based on FGM data during week 6 of radiotherapy and temozolomide therapy

    Secondary Outcome Measures

    1. Area under the curve for glycemic exposure and variability [baseline, week 1, 2, 3, 4, 5, 6, 10-13, 3 months]

      Glucose levels measured using FGM vs conventional clinical measures (e.g. capillary blood glucose)

    2. Neurocognitive Function [Baseline]

      To explore the association between glycemia and neurocognitive functions patients will undergo standardized tests

    3. Neurocognitive Function [After week 10 and before week 13]

      To explore the association between glycemia and neurocognitive functions patients will undergo standardized tests

    4. Neurocognitive Function [3 month follow up visit]

      To explore the association between glycemia and neurocognitive functions patients will undergo standardized tests

    5. prevalence of sensor site problems [From baseline to week 6 - the time from sensor insertion through completion of study intervention]

      infection, irritation, and secondary complication in the study cohort

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Adult patients (> 18 years old) with a new histologically-confirmed diagnosis of glioblastoma who are planned to receive a 6-week course of concurrent radiation and temozolomide

    • Has evidence of random glucose of at least 7.8 mmol/L or fasting blood glucose of at least 6.1 mmol/L (meeting criteria for oral diabetic medications)

    • Able to provide informed consent

    • Able to understand and follow instructions regarding self-administered capillary glucose measurements

    Exclusion Criteria:
    • Contraindication to MRI with gadolinium

    • Taking anti-hyperglycemic medications at the time of study eligibility screen

    • Unable to participate in neurocognitive evaluation in English

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Princess Margaret Cancer Centre Toronto Ontario Canada M5G 2M9

    Sponsors and Collaborators

    • University Health Network, Toronto
    • Sinai Health System

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University Health Network, Toronto
    ClinicalTrials.gov Identifier:
    NCT03235934
    Other Study ID Numbers:
    • 15-9329
    First Posted:
    Aug 1, 2017
    Last Update Posted:
    Oct 25, 2021
    Last Verified:
    Oct 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by University Health Network, Toronto
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 25, 2021