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Protocol for a randomised controlled trial of the effect of dapagliflozin, metformin and exercise on glycaemic variability, body composition and cardiovascular risk in prediabetes (the PRE-D Trial)
- Source :
- BMJ Open, Færch, K, Amadid, H, Nielsen, L B, Ried-Larsen, M, Karstoft, K, Persson, F & Jørgensen, M E 2017, ' Protocol for a randomised controlled trial of the effect of dapagliflozin, metformin and exercise on glycaemic variability, body composition and cardiovascular risk in prediabetes (the PRE-D Trial) ', BMJ Open, vol. 7, no. 5, e013802 . https://doi.org/10.1136/bmjopen-2016-013802
- Publication Year :
- 2017
-
Abstract
- INTRODUCTION: The primary aim of this study is to compare the efficacy of three short-term glucose-lowering interventions (exercise, metformin and dapagliflozin) on glycaemic variability in overweight or obese men and women with elevated diabetes risk (ie, prediabetes, defined as haemoglobin A1c (HbA1c)39-47 mmol/mol / 5.7%-6.4%). The secondary aims are to investigate the effects of the interventions on body composition and cardiometabolic risk factors.METHODS AND ANALYSIS: The Pre-D Trial is an investigator-initiated, randomised, controlled, parallel, open-label, superiority trial. The study aims to assign 120 participants in a 1:1:1:1 ratio to receive one of four interventions for 13 weeks: (1) dapagliflozin (10 mg once daily); (2) metformin (850 mg twice daily); (3) exercise (interval training, 5 days a week, 30 min per session); or (4) control (lifestyle advice). After the 13 weeks of intervention, a follow-up period of 13 weeks will follow to study the long-term effects of the interventions. The primary endpoint is reduction from baseline to end-of treatment (13 weeks) in mean amplitude of glycaemic excursions measured by continuous glucose monitoring. The secondary endpoints include concomitant changes in various measures of glucose metabolism, body weight, cardiorespiratory fitness, blood pressure, plasma lipids, objectively measured physical activity and dietary intake.ETHICS AND DISSEMINATION: The study protocol has been approved by the Ethics Committee of the Capital Region and the Danish Medicines Agency. Approval of data and biobank storage has been obtained from the Danish Data Protection Board. The study will be carried out according to the Declaration of Helsinki and to the regulations for good clinical practice. The results from this trial will allow a number of research questions concerning the effect of exercise versus dapagliflozin or metformin in HbA1c-defined prediabetes to be addressed.TRIAL REGISTRATION: NCT02695810.
- Subjects :
- Male
Denmark
030204 cardiovascular system & hematology
Overweight
Interval training
law.invention
chemistry.chemical_compound
0302 clinical medicine
Superiority Trial
PREVENTIVE MEDICINE
Randomized controlled trial
Glucosides
law
Risk Factors
Clinical endpoint
Protocol
Medicine
Prediabetes
Dapagliflozin
DIABETES & ENDOCRINOLOGY
General Medicine
Middle Aged
Metformin
Diabetes and Endocrinology
Cardiovascular Diseases
Research Design
Body Composition
Female
medicine.symptom
PUBLIC HEALTH
Adult
medicine.medical_specialty
Diabetes risk
030209 endocrinology & metabolism
Prediabetic State
03 medical and health sciences
Double-Blind Method
Journal Article
Humans
Hypoglycemic Agents
Obesity
Benzhydryl Compounds
Exercise
Aged
Glycated Hemoglobin
business.industry
Body Weight
medicine.disease
chemistry
Physical therapy
business
Subjects
Details
- ISSN :
- 20446055
- Volume :
- 7
- Issue :
- 5
- Database :
- OpenAIRE
- Journal :
- BMJ open
- Accession number :
- edsair.doi.dedup.....ea41b907b1a88684ab31d017bc9ed6b4
- Full Text :
- https://doi.org/10.1136/bmjopen-2016-013802