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OpenTrials
Completed

NCT Number: NCT01492218

Observational Study With Mixtard® 30 NovoLet® to Assess Patient Satisfaction

This study is conducted in Asia. The aim of this study is to assess patient satisfaction after switching to biphasic human insulin 30 treatment using the NovoLet® insulin device as treatment for diabetes mellitus under normal clinical practice setting.

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Key information

Sex eligibility

All sexes

Study type

Observational

Primary location

Novo Nordisk Investigational Site

Manila, 1605, Philippines

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diabetes mellitus (type 1 or type 2)
  • Patient not presently using Mixtard® 30 NovoLet®

Treatment and study plan

biphasic human insulin 30

Drug

Administered via the NovoLet® device and according to the instructions in the product insert or as instructed by the physician. Individually adjusted dosage as instructed by the physician.

Primary outcomes

  1. Change in Diabetes Treatment Satisfaction Questionnaire (DTSQ) score

Secondary outcomes

  1. Adverse events

  2. Technical complaints of NovoLet® device

Sponsors and collaborators

Lead sponsor

Novo Nordisk A/S

Industry

Registry information

Official study title

A Prospective, Open-labelled, Non-controlled Observational Study to Assess Patient Satisfaction, Physician Acceptability and Safety of Mixtard® 30 NovoLet® for the Treatment of Diabetes Mellitus

Important dates

Study start
2004
Primary completion
2004
Study completion
2004
First posted
Dec 14, 2011
Registry last updated
Feb 28, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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