The aim of the current pilot study is to investigate the prevalence of (symptomatic) hypoglycaemia in frail elderly patients with type 2 diabetes treated with sulfonylurea and metformin, and to gather data for a full-scale hypothesis-testing study.…
ID
Bron
Verkorte titel
Aandoening
Older well-controlled patients with type 2 Diabetes Mellitus
Hypoglycaemia / hypoglycemie
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Hypoglycaemia < 3.0 mmol/L of at least 15 minutes.
Achtergrond van het onderzoek
The current national primary care guideline recommends gliclazide as the second pharmacological step in diabetes management. Unfortunately, there is very limited data regarding hypoglycaemia rates in elderly patients using SUs. As more than one quarter of the type 2 diabetes population in the Netherlands is older than 75 years, differences in the frequency of hypoglycaemic events between SUs could be relevant. These events can be easily reported by the CGMS. Previous studies with CGMS already showed us that (asymptomatic) hypoglycaemic events are easily missed in elderly patients. However, these studies did not use an appropriate control group. Data regarding the effects of SUs, and specifically gliclazide, are needed for confirming the safety of gliclazide in frail elderly patients treated in primary care.
Doel van het onderzoek
The aim of the current pilot study is to investigate the prevalence of (symptomatic) hypoglycaemia in frail elderly patients with type 2 diabetes treated with sulfonylurea and metformin, and to gather data for a full-scale hypothesis-testing study. The aim of this large powered study will be to compare differences in the prevalence of hypoglycemic events between the most commonly used sulfonylurea derivatives (SUs), glimepiride and gliclazide.
Onderzoeksopzet
Visit 1: inclusion, informed consent, blood drawn for HbA1c measurement, Groningen Frailty index.
Visit 2 (day 1): baseline measurements, blood pressure measurements, CGMS implanted.
Day 1: CGMS implanted after breakfast, SMBG (4-5x);
Day 2: SMBG (N, VL, VA, VS);
Day 3: SMBG (N, VL, VA, VS);
Day 4: SMBG (N, VL, VA, VS);
Visit 3 (day 5): removal of CGMS, collection of patient diary.
Onderzoeksproduct en/of interventie
N/A
Algemeen / deelnemers
Wetenschappers
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
- known type 2 diabetes mellitus;
- >70 years old;
- HbA1c <58 mmol/mol;
- Groningen Frailty Indicator score ≥4;
- treatment with:
• metformin only (any dosage); or
• metformin (any dosage) + gliclazide (any dosage); or
• metformin (any dosage) + glimepiride (any dosage).
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
- insufficient knowledge of the Dutch language to understand the requirements of the study;
- advanced dementia;
- known anemia;
- terminally ill or an estimated life expectancy <3 months.
Opzet
Deelname
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Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
Register | ID |
---|---|
NTR-new | NL4829 |
NTR-old | NTR4952 |
CCMO | NL51201.075.14 |
OMON | NL-OMON42250 |