Insulin Degludec and Symptomatic Nocturnal Hypoglycaemia

Type 1 Diabetes Mellitus Clinical Trial

— HypoDeg  

Official title:

The Effect of Insulin Degludec on Risk of Symptomatic Nocturnal Hypoglycaemia in Subjects With Type 1 Diabetes and High Risk of Nocturnal Severe Hypoglycaemia

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02192450
• Other study ID #: HypoDeg
• Status: Completed
• Phase: Phase 4
• Start date: January 2015
• Est. completion date: February 28, 2019

Study information

• Verified date: June 2019
• Source: Nordsjaellands Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to determine whether insulin degludec compared to insulin glargine can reduce the risk of symptomatic nocturnal hypoglycaemia in subjects with the greatest potential benefit from optimised insulin treatment, which are patients with type 1 diabetes and high risk of nocturnal severe hypoglycaemia.

Description:

Background: Insulin degludec is a novel insulin analogue that may reduce the risk of mild nocturnal hypoglycaemia in type 1 diabetes. Patients with type 1 diabetes and recurrent severe hypoglycaemia (high risk patients) are also burdened by nocturnal hyoglycaemia (mild and silent). These episodes may contribute to the developement of hormonal counterregulatory failure and hypoglycaemia unawareness, which in turn increases the risk of further hypoglycaemic episodes, especially epiosdes of severe hypoglycaemia.The effect of insulin degludec on risk of mild nocturnal hypoglycaemia in subjects with type 1 diabetes and high risk of severe hypoglycaemia compared to insulin glargine is to be investigated.

Study design and intervention: A controlled, cross-over multi-centre study in a Prospective, Randomised, Open, Blinded Endpoint (PROBE) design. Each treatment period last for 12 months. Patients will be randomised to treatment with basal-bolus therapy with insulin aspart/degludec or insulin aspart/glargine in random order. Endpoints will be assessed during the last 9 months of each treatment arm.

Subjects: 175 type 1 diabetic patients with a history of one or more episodes of nocturnal severe hypoglycaemia during the proceeding two years.

Method: Patients will record all events of symptomatic (mild), asymptomatic (silent) and severe hypoglycaemia in a diary. All events of symptomatic nocturnal and severe hypoglycaemia must also be reported by telephone within 24 hours. Patients will be instructed to do and record self-monitored blood glucose (SMBG) i.e. 4-point profiles twice per week (blood glucose before breakfast, before lunch, before dinner and before bedtime).

Outcomes: See "Outcome Measures". Concerning the primary endpoint all possible symptomatic nocturnal hypoglycaemic episodes will be adjudicated by an independent endpoint committee consisting of diabetes specialists blinded to the individual patient insulin regimen.

Safety: Adverse reactions

Recruitment information / eligibility

• Status: Completed
• Enrollment: 149
• Est. completion date: February 28, 2019
• Est. primary completion date: February 28, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Type 1 diabetes > 5 years

• One or more episodes of nocturnal severe hypoglycaemia during the preceding two years

• Treated with multiple dose insulin injection (>2) or insulin pump. Both human insulin and insulin analogues are allowed

• Willingness to a once daily (OD) regimen concerning insulin degludec and insulin glargine

• Willingness to do self-monitoring of blood glucose (SMBG) and keep a diary

• Signed informed consent

Exclusion Criteria:

• History of primary and secondary adrenal insufficiency, growth hormone deficiency, or untreated myxoedema

• History of unstable angina or major cardiovascular events (myocardial infarction, coronary re-vascularisation, transient ischaemic attack, or stroke within the last three months)

• Heart failure, New York Heart Association (NYHA) class IV

• History of malignancy unless a disease-free period exceeding five years

• History of alcohol or drug abuse

• Treatment with glucose lowering agent(s) other than insulin

• Pregnant or lactating women

• Women of childbearing potential who are not using chemical (P-pills or gestagen depots) or mechanical (intra-uterine device) contraception

• Participation in another investigational drug study within the last 3 months

• Inability to understand the informed consent

• HbA1c > 86 mmol/mol (10%)

• Shifting working hours

Related Conditions & MeSH terms

• Diabetes Mellitus
• Diabetes Mellitus, Type 1
• Hypoglycemia
• Nocturnal Hypoglycemia
• Recurrent Severe Hypoglycaemia
• Type 1 Diabetes Mellitus

Intervention

Drug:
• Insulin aspart/glargine

• Insulin aspart/degludec

Locations

Country	Name	City	State
Denmark	Nordsjaellands Hospital	Hilleroed

Sponsors (8)

Lead Sponsor	Collaborator
Nordsjaellands Hospital	Aarhus University Hospital, Copenhagen University Hospital, Denmark, Hvidovre University Hospital, Odense University Hospital, Steno Diabetes Center Copenhagen, Sydvestjysk Hospital, Zealand University Hospital

Country where clinical trial is conducted

Denmark, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Symptomatic nocturnal hypoglycaemia		9 months (3-12) of each treatment period
Secondary	Severe hypoglycaemia (total, night-time, daytime)		9 months (3-12) of each treatment period
Secondary	Any nocturnal hypoglycaemia (incl. asymptomatic/silent events)		9 months (3-12) of each treatment period
Secondary	Any daytime hypoglycaemia (symptomatic, asymptomatic/silent and severe)		9 months (3-12) of each treatment period
Secondary	Any CGM recorded hypoglycaemia (symptomatic, asymptomatic/silent and severe)		2 x 6 days in each treatment arm
Secondary	Any in-hospital nocturnal hypoglycaemia (incl. asymptomatic/silent events)		2 overnight stays in each treatment arm
Secondary	Change in HbA1c		From baseline to after 12 months of treatment
Secondary	Change in glycaemic variability		4 x overnight stays and 4 x 6 days of CGM
Secondary	Insulin doses		End of each treatment period
Secondary	Quality of life incl. pre-depression scale		At baseline, cross-over and after 24 months