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Completed

NCT Number: NCT03721874

Effects of 2 Weeks Treatment With Dapagliflozin in Subjects With an Impaired Glucose Homeostasis on Nocturnal Substrate Oxidation

The purpose of this study is to investigate the effect of 2 weeks dapagliflozin treatment in individuals with a disrupted glucose homeostasis on the switch between carbohydrate and lipid oxidation during the night

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Key information

Age range

40 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Maastricht University and Medical Centre

Maastricht, Limburg, 6200 MD, Netherlands

About this study

To investigate if dapagliflozin improves nocturnal substrate oxidation expressed as respiration quotient (RQ) during the sleeping period in comparison with placebo after 2-weeks double blind treatment in subjects with a disrupted glucose homeostasis.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Provision of signed and dated informed consent prior to any study specific procedures.
  • Males aged ≥ 40 and ≤ 75 years and post-menopausal women (defined as at least 1 year post cessation of menses) aged ≥ 50 and ≤ 75 years
  • Body mass index (BMI) ≥ 27 and ≤ 38 kg/m2.
  • Sedentary lifestyle (not more than 3 hours of programmed exercise per week).
  • Stable dietary habits.
  • Impaired glucose homeostasis based on one or a combination of the following criteria:
  • Impaired Glucose Tolerance (IGT): plasma glucose values ≥ 7.8 mmol/l and ≤ 11.1 mmol/l 120 minutes after consumption of the glucose drink during the 2h, 3-point OGTT.
  • Impaired Fasting Glucose (IFG): fasting plasma glucose ≥ 6.1 mmol/l and ≤ 6.9 mmol/l.
  • Insulin Resistance: glucose clearance rate ≤ 360 ml/kg/min, as calculated by Oral Glucose Insulin Sensitivity 120 (OGIS120) model based on the 2h, 3-point OGTT.
  • HbA1c ≥ 5.7% and ≤ 6.4%.

Exclusion criteria

  • Clinical diagnosis of Type 1 or 2 Diabetes Mellitus.
  • Active cardiovascular disease: participants who experienced a heart attack in the last year, or participants who are currently under regular control of a physician for a heart condition.
  • Weight gain or loss > 5 kg in the last 3 months, ongoing weight-loss diet (hypocaloric diet) or use of weight loss agents.
  • Regular smoking and other regular nicotine use.
  • Anaemia.
  • Uncontrolled hypertension.
  • Clinically significant out of range values of serum levels of either alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP) in the Investigator's opinion.
  • Unstable or rapidly progressing renal disease or estimated Glomerular Filtration Rate (eGFR) <60 mL/min (Cockcroft-Gault formula).
  • Use of anti-coagulant treatment and other concomitant medication will be evaluated on a case to case basis with a general physician.
  • Use of medication such as oral glucocorticoids, anti-estrogens or other medications that are known to markedly influence insulin sensitivity.
  • Use of loop diuretics.
  • Intake of dietary supplements except multi-vitamins and minerals.
  • Alcohol consumption of > 14 drinks per week for women and > 21 drinks per week for men (1 drink = 35 cl beer, 14 cl wine or 4 cl hard liquor).
  • Known hypersensitivity to dapagliflozin or any of the excipients of the product.
  • For women only - currently pregnant (confirmed with positive pregnancy test) or breast-feeding.
  • Participation in another biomedical study within 1 month before the screening visit.
  • Any contraindication for MRI scanning.
  • Participants who do not want to be informed about unexpected medical findings, or do not wish that their physician be informed about coincidental findings, cannot participate in the study.

Treatment and study plan

Dapagliflozin 10mg

Drug

The study consist of 2 weeks treatment period 1, 6-8 weeks wash-out period and 2 weeks treatment period 2.

The subject may be administered dapagliflozin 10 mg during Period 1 or Period 2.

Placebo matching to Dapagliflozin 10 mg

Drug

The study consist of 2 weeks treatment period 1, 6-8 weeks wash-out period and 2 weeks treatment period 2.

The subject may be administered placebo during Period 1 or Period 2.

Primary outcomes

  1. Change in nightly substrate oxidation measured as respiration quotient (RQ) during the sleeping period

    Time frame: From screening to day 14

    Comparison of dapagliflozin versus placebo after 14 days of treatment on nightly substrate oxidation as measured by respiratory quotient (VCO2/VO2) during the sleeping period.

Secondary outcomes

  1. Change in morning and late afternoon hepatic glycogen content

    Time frame: 1 hour

    Comparison of dapagliflozin versus placebo after 14 days of treatment on hepatic glycogen content determined by non-invasive 13C-MRS (magnetic resonance spectroscopy) in the morning and evening

  2. Change in 24h substrate oxidation as determined by indirect calorimetry in a whole-body respiratory chamber and based on urinary nitrogen excretion

    Time frame: 24 hours

    Comparison of dapagliflozin versus placebo after 14 days of treatment on 24h substrate oxidation as determined by indirect calorimetry in a whole-body respiratory chamber and based on urinary nitrogen excretion

  3. Change in 24h plasma markers

    Time frame: 24 hours

    Comparison of dapagliflozin versus placebo after 14 days of treatment on 24h plasma markers including plasma glucose, NEFA, total amino acid levels incl BCAA levels, insulin and glucagon

  4. Change in muscle mitochondrial function

    Time frame: 60 minutes

    Comparison of dapagliflozin versus placebo after 14 days of treatment on muscle mitochondrial function as determined by high resolution respirometry

  5. Change in intrahepatic lipid content and composition

    Time frame: 45 minutes

    Comparison of dapagliflozin versus placebo after 14 days of treatment on intrahepatic lipid content and composition as determined by non-invasive 1H-MRS (magnetic resonance spectroscopy )

  6. Change in intramyocellular lipid content and composition - including acylcarnitine levels

    Time frame: 45 minutes

    Comparison of dapagliflozin versus placebo after 14 days of treatment on intramyocellular lipid content and composition-including acylcarnitine levels as determined in muscle biopsies

  7. Change in muscle glycogen content

    Time frame: 45 minutes

    Comparison of dapagliflozin versus placebo after 14 days of treatment on muscle glycogen content as determined biochemically in muscle biopsies

  8. Change in systolic and diastolic blood pressure

    Time frame: 45 minutes

    Comparison of dapagliflozin versus placebo after 14 days of treatment on systolic and diastolic blood pressure

Sponsors and collaborators

Lead sponsor

Maastricht University

Other

Collaborators

  • AstraZeneca

Registry information

Official study title

MaasFlex: Double-Blind, Randomized, Phase IV, Mechanistic, Placebo-Controlled, Cross-Over, Single-Center Study to Evaluate the Effects of 2 Weeks Dapagliflozin Treatment on Nocturnal Substrate Oxidation, Glucose Metabolism and Muscle Mitochondrial Function in Individuals With Impaired Glucose Homeostasis

Acronym: MaasFlex

Important dates

Study start
2019
Primary completion
2021
Study completion
2021
First posted
Oct 26, 2018
Registry last updated
Aug 19, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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