Placebo Clinical Trial
— DE-CAFOfficial title:
Does Combined Caffeine and Carbohydrate Ingestion Counter the Exercise-mediated Fall in Glycaemia in Individuals With Type 1 Diabetes on Insulin Degludec? The DE-CAF Study
Verified date | March 2023 |
Source | University Hospital Inselspital, Berne |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This project will aim to investigate the clinical efficacy and metabolic effects of a pre-exercise dose of caffeine with a low (10g) dose of carbohydrate (CAF+lowCHO) without modification of insulin degludec on exercise metabolism in people with T1D.
Status | Completed |
Enrollment | 21 |
Est. completion date | February 2, 2023 |
Est. primary completion date | February 2, 2023 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 45 Years |
Eligibility | Inclusion Criteria: - Type 1 diabetes for =1 year and negative C-peptide (<100pmol/l) - Male and female aged 18-45 years old - HbA1c <8.5% (69 mmol/mol) based on analysis from the central laboratory unit of Bern University Hospital - Using multiple daily injections - Using insulin degludec (Tresiba; Novo Nordisk A/S, Bagsværd, Denmark) as basal insulin for a minimum of 3 months - Written informed consent - Able and willing to adhere to safe contraception during the study and for 2 weeks after completion of the study. Safe contraception comprises double barrier methods (hormonal contraception [like: oral contraceptive pills or intrauterine contraceptive devices] together with a mechanical barrier [like: condom, diaphragm]). Exclusion Criteria: - Physical or psychological disease likely to interfere with the normal conduct of the study as judged by the investigator - Continuous subcutaneous insulin infusion (using an insulin pump) - Hypoglycaemic unawareness (Gold likert score =4) or having experienced any episode of a severe hypoglycaemic event within the last 6 months (i.e. need of third-party assistance). - Current treatment with drugs known to interfere with metabolism e.g. systemic corticosteroids, SGLT2 inhibitors, Glucagon like 1 peptide- receptor agonists, or metformin. - Relevant diabetic complications as judged by the investigator and based on medical record check (no cardiovascular disease and no significant microvascular disease) - Microalbuminuria (as defined by area under the curve >30 mg/g) - Body mass index more than or equal to 30 kg/m2 - Uncontrolled hypertension (>180/100 mmHg) - Pregnant or planning to become pregnant during the study period (females only) - Breastfeeding |
Country | Name | City | State |
---|---|---|---|
Switzerland | Department of Diabetes, Endocrinology, Nutritional Medicine and Metabolism, Inselspital, Bern University Hospital and University of Bern, Bern, Switzerland | Bern |
Lead Sponsor | Collaborator |
---|---|
University Hospital Inselspital, Berne |
Switzerland,
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* Note: There are 25 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Hypoglycaemia | Time to hypoglycaemia (plasma glucose <3.9mmol/l) during the 60 min of exercise | 60 minutes from start of exercise | |
Secondary | Change in blood glucose concentration | Change in blood glucose concentration, calculated based on the participants' glucose at the start of exercise and the last value measured at the end of exercise. If the exercise is stopped early because of hypoglycaemia, the last exercise glucose value will be used for analysis. | 60 minutes from start of exercise | |
Secondary | Mean glucose concentration | Mean glucose concentration during the exercise bout | 60 minutes from start of exercise | |
Secondary | Area under the glucose curve | Area under the glucose curve during exercise | 60 minutes from start of exercise | |
Secondary | %-Time in target glycaemic range during recovery | Time in target glycaemic range (4-10 mmol/l) in the recovery period and overnight | 24 hours | |
Secondary | %-Time in target glycaemic range during exercise | Time in target glycaemic range (4-10 mmol/l) during exercise | 60 minutes | |
Secondary | Incidence of hypoglycaemia during exercise | Incidence of hypoglycaemia (=3.9 mmol/l) during exercise | 60 minutes | |
Secondary | Incidence of hypoglycaemia during recovery | Incidence of hypoglycaemia (=3.9 mmol/l for 15 min or more) during the 24 hour post exercise recovery period | 24 hours | |
Secondary | % Time below target range (< 3.9 mmol/L) during nighttime after exercise | The % time of glucose sensor measurements < 3.9 mmol/L in the night following the exercise visits will be documented | 12:00 am until 06:00 am after each exercise visit | |
Secondary | % Time below target range (> 10.0 mmol/L) during nighttime after exercise | The % time of glucose sensor measurements > 10.0 mmol/L in the night following the exercise visits will be documented | 12:00 am until 06:00 am after each exercise visit | |
Secondary | Mean sensor glucose overnight | The mean sensor glucose in mmol/L in the nights following the exercise visits will be documented | 12:00 am until 06:00 am after each exercise visit | |
Secondary | Area under the glucose curve post exercise | The sensor glucose in mmol/L within 30 minutes following the exercise visits will be documented and the area under the curve will be calculated | 30 minutes after stop of exercise |
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