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OpenTrials
Completed

NCT Number: NCT01542060

Efficacy and Safety of Biphasic Insulin Aspart 30 for the Treatment of Type 2 Diabetes Mellitus

This study is conducted in Asia. The aim of this observational study is to collect efficacy and safety data of biphasic insulin aspart (NovoMix® 30) in type 2 diabetes under normal clinical practice conditions.

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Key information

Sex eligibility

All sexes

Study type

Observational

Primary location

Amman, 11844, Jordan

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Subjects from hospitals or clinics, diagnosed with type 2 diabetes mellitus

Treatment and study plan

biphasic insulin aspart 30

Drug

Administered via an insulin injection device. Dosages varied according to individual patients' medical requirement as determined by their attending clinician

Primary outcomes

  1. HbA1c (glycosylated haemoglobin)

Secondary outcomes

  1. FBG (Fasting Blood Glucose)

  2. Quality of life assessed through the WHO-DTSQ (World Health Organization-Diabetes Treatment Satisfaction Questionnaire)

  3. Incidence of adverse events

  4. Incidence of hypoglycaemic episodes

Sponsors and collaborators

Lead sponsor

Novo Nordisk A/S

Industry

Registry information

Official study title

A Clinical Experience Programme to Collect Data on the Safety and Efficacy of NovoMix® 30 in the Treatment of Patients With Type 2 Diabetes in Jordan

Important dates

Study start
2004
Primary completion
2004
Study completion
2004
First posted
Mar 1, 2012
Registry last updated
Apr 12, 2012

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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