Comparison of Insulin Detemir and NPH Insulin Given Once Daily in Ageing Subjects With Type 2 Diabetes (3L)

Novo Nordisk

Status and phase

Terminated

Phase 4

Conditions

Diabetes

Diabetes Mellitus, Type 2

Treatments

Drug: insulin NPH

Drug: insulin detemir

Study type

Interventional

Funder types

Industry

Identifiers

NCT00506662

NN304-1808

2006-006589-41 (EudraCT Number)

Details and patient eligibility

About

This trial is conducted in Europe. The aim of the trial is to compare insulin detemir once daily to NPH insulin once daily as measured by blood sugar control in ageing subjects with type 2 diabetes naive to previous insulin therapy.

Full description

Novo Nordisk has decided to discontinue the trial as it will not be possible to recruit the required number of patients. The discontinuation is based on an analysis of the significant delay in recruitment of patients which is likely to have a negative impact on the validity of the trial.

Enrollment

86 patients

Sex

All

Ages

70+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Type 2 diabetes
Insulin naive
Treatment with oral anti-diabetic drugs (OADs) for at least 3 months and not achieving therapeutic targets
HbA1c between 8% - 10.5%

Exclusion criteria

Secondary diabetes, MODY (Maturity Onset Diabetes of the Young)
Previous treatment with insulin (except for short-term treatment with insulin for intercurrent illness as judged by the Investigator)
Proliferative retinopathy, maculopathy requiring treatment,
Hypoglycaemia unawareness as judged by the Investigator, recurrent major hypoglycaemia
End stage liver disease (increased liver enzymes 4 fold), end stage renal disease assessed by MDRD (Modification of Diet in Renal Disease) less than 30 ml/min or dialysed patient, acute heart failure, any acute cardiovascular event or cerebrovascular event less than 6 months
Acute disease with poor prognosis
History of alcoholism, drug abuse, or psychiatric disease or personality disorders likely to invalidate voluntary consent or to prevent good compliance with the trial protocol
Mental incapacity, unwillingness or language barrier precluding adequate understanding or co-operation (patients having a score of less than 15 in a previous MMSE (Mini-Mental State Examination) in the last six months) and any conditions as judged by the investigator
Legal incapacity or limited legal capacity (patients under guardianship or curatorship)
Concomitant medication for Alzheimers treatment (Memantine, Anticholinesterasique treatment)
Participation in another clinical trial less than one month before inclusion in this trial
Illness requiring repeated hospitalisation
Known or suspected allergy to the insulin or any compositional component
Anticipated change or new use in concomitant medication known to interfere with glucose metabolism, such as systemic corticotherapy more than 5 mg/day (prednisone)
Any other condition that the Investigator feels would interfere with trial participation or evaluation of results
Terminal illness