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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00569998
Other study ID # MS236-1544
Secondary ID
Status Completed
Phase Phase 3
First received December 4, 2007
Last updated January 18, 2017
Start date August 2003
Est. completion date February 2004

Study information

Verified date January 2017
Source Novo Nordisk A/S
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

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

Study Design


Intervention

Device:
NovoPen™ 4

NovoPen® 3


Locations

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

Sponsors (1)

Lead Sponsor Collaborator
Novo Nordisk A/S

Countries where clinical trial is conducted

Austria,  Germany,  Italy,  Netherlands,  United Kingdom, 

References & Publications (2)

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

Outcome

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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