Diabetes Mellitus, Type 2 Clinical Trial
Official title:
An Open-label, Multi-centre, Multi-national, Comparative, Randomised, Cross-over Trial Evaluating Preference as Well as Performance, Acceptance, Handling and Safety of NovoPen™ 4 (MS236) Versus NovoPen 3® in Insulin Treated Diabetic Patients
Verified date | January 2017 |
Source | Novo Nordisk A/S |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This trial is conducted in Europe. The aim of this trial is to compare two insulin delivery pens in the everyday life setting of patients with diabetes treated with insulin.
Status | Completed |
Enrollment | 208 |
Est. completion date | February 2004 |
Est. primary completion date | February 2004 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 9 Years and older |
Eligibility |
Inclusion Criteria: - Type 1 or type 2 diabetes mellitus for at least 12 months - Adults at least 18 years - Children/adolescents between 9-18 years - HbA1c lesser than or equal to 11.0% Exclusion Criteria: - Known or suspected alcohol or drug abuse - Patients who are not able to read the user manual (may wear glasses if needed) - Hypoglycaemic unawareness as judged by the investigator - Visual and/or dexterity impairments as judged by the investigator |
Country | Name | City | State |
---|---|---|---|
Austria | Novo Nordisk Investigational Site | Wien | |
Austria | Novo Nordisk Investigational Site | Wien | |
Germany | Novo Nordisk Investigational Site | Köln | |
Germany | Novo Nordisk Investigational Site | Leverkusen | |
Germany | Novo Nordisk Investigational Site | München | |
Germany | Novo Nordisk Investigational Site | Speyer | |
Germany | Novo Nordisk Investigational Site | St. Ingbert | |
Germany | Novo Nordisk Investigational Site | Völklingen | |
Italy | Novo Nordisk Investigational Site | Catania | |
Italy | Novo Nordisk Investigational Site | Palermo | |
Italy | Novo Nordisk Investigational Site | Parma | |
Italy | Novo Nordisk Investigational Site | Roma | |
Italy | Novo Nordisk Investigational Site | Torino | |
Netherlands | Novo Nordisk Investigational Site | Almere | |
Netherlands | Novo Nordisk Investigational Site | Amsterdam | |
Netherlands | Novo Nordisk Investigational Site | Den Haag | |
Netherlands | Novo Nordisk Investigational Site | Heerlen | |
Netherlands | Novo Nordisk Investigational Site | Rotterdam | |
Netherlands | Novo Nordisk Investigational Site | Veldhoven | |
United Kingdom | Novo Nordisk Investigational Site | Belfast | |
United Kingdom | Novo Nordisk Investigational Site | Belfast | |
United Kingdom | Novo Nordisk Investigational Site | Leeds | |
United Kingdom | Novo Nordisk Investigational Site | Sidcup |
Lead Sponsor | Collaborator |
---|---|
Novo Nordisk A/S |
Austria, Germany, Italy, Netherlands, United Kingdom,
Goke B, Gamba S, Erdtsieck RJ, Gilbey S, Schober E, Lytzen L, Kolaczynski M. NovoPen 4 offers superior performance, handling and acceptance compared with NovoPen 3 in insulin-treated diabetes patients. Diabetes Technology and Therapeutics 2005; 7 (2): 379
Kolaczynski M, Chayer D. NovoPen® 4: perceived as superior in handling and acceptance versus HumaPen® Ergo and OptiPen® Pro in patients and healthcare professionals. Diabetes Technology & Therapeutics 2005; 7 (2): 390
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Evaluation of overall pen preference | after 12 weeks of treatment | ||
Secondary | HbA1c | |||
Secondary | Adverse device effects | |||
Secondary | Adverse events |
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