Diabetes Type 2, Treatment During Ramadan
Conditions
Keywords
Diabetes type 2, Fasting, Ramadan, Insulin analogues
Brief summary
Fasting during the Ramadan is one of the five pillars of Islam and is a mandatory duty for all healthy adult Muslims. Fasting is considered safe in young healthy subjects but it can induce harmful effects and complications in patients with diabetes. Several studies have demonstrated that patients with type 2 diabetes are prone to hypo and hyper glycemia during fasting. When treating diabetic patients with a treatment guideline the rate of these complications can be reduced. Little data is available on patients with type 2 diabetes treated with insulin. The investigators therefore propose to assess the effect of a protocol containing detemir (levemir) and a premix of insulin aspart (NovoMix70) on glucose control in patients with type 2 diabetes during the Ramadan and to compare this regimen to the standard care patients receive during this period. The investigators assume that patients receiving the intervention will have better glucose control during the Ramadan compared to patients receiving the standard care. As approximately 45 million Muslims suffer from type 2 diabetes and most of them fast during the Ramadan the results of this intervention may be significant and may improve the care of these patients allowing Muslims to respect their religious obligations without compromising their health.
Interventions
Insulin analogs will be used: Levemir and NovoMix70. The daily insulin dose will be calculated as follows: Sixty percent of the total daily dose will be used as the beginning daily dose at the first day of fasting. Sixty percent of the daily dose will be given as NovoMix70 before the Eftar (the main meal in the evening that breaks the fast). Forty percent of the amount will be given as Levemir (Early in the morning before the beginning of fasting.
Standard of care during Ramadan according to physicians decision
Sponsors
Study design
Eligibility
Inclusion criteria
All of these criteria should be present. 1. Patients with a diagnosis of type 2 diabetes treated with insulin (premix preparations or basal and rapid acting insulin) with or without metformin and/or a sulfonylurea drug for at least three months 2. HbA1c in the past three months ≤ 10% 3. Being capable, and willing, to perform self blood glucose monitoring and use a patient diary as required 4. Age \> 18 years
Exclusion criteria
Any of the following: 1. Patients with a diagnosis of type 1 diabetes 2. Hypoglycemia unawareness 3. Hypersensitivity to levemir 4. Hypersensitivity to NovoMix70 5. Creatinine \> 2.5 mg/l 6. AST and or ALT \> 1.5 times the upper limit 7. Pregnancy 8. Mental incapacity, unwillingness or language barrier precluding adequate understanding of the study protocol or cooperation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Difference in mean 4-point SMBG during days 23-30 of treatment between the two groups. | days 23-30 of treatment |
Countries
Israel