Clinical Trial Details
Trial ID: | L6663 |
Source ID: | NCT00184561 |
Associated Drug: | Biphasic Insulin Aspart |
Title: | Effectiveness and Safety of Biphasic Insulin Aspart 70/30 in Subjects With Type 2 Diabetes |
Acronym: | |
Status: | COMPLETED |
Study Results: | NO |
Results: | |
Conditions: | Diabetes|Diabetes Mellitus, Type 2 |
Interventions: | DRUG: biphasic insulin aspart |
Outcome Measures: | Primary: Change in HbA1c, After 24 weeks of treatment | Secondary: Adverse events|Weight change|Fasting blood glucose|Hypoglycaemic episodes|2-hour postprandial blood glucose|after 24 weeks of treatment. |
Sponsor/Collaborators: | Sponsor: Novo Nordisk A/S |
Gender: | ALL |
Age: | ADULT, OLDER_ADULT |
Phases: | PHASE4 |
Enrollment: | 321 |
Study Type: | INTERVENTIONAL |
Study Designs: | Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: NONE|Primary Purpose: TREATMENT |
Start Date: | 2005-07 |
Completion Date: | 2006-07 |
Results First Posted: | |
Last Update Posted: | 2017-01-06 |
Locations: | Novo Nordisk Investigational Site, Beijing, Beijing, 100029, China|Novo Nordisk Investigational Site, Beijing, Beijing, 100730, China|Novo Nordisk Investigational Site, Guangzhou, Guangdong, 510120, China|Novo Nordisk Investigational Site, Wuhan, Hubei, 430022, China|Novo Nordisk Investigational Site, Nanjing, Jiangsu, 210008, China|Novo Nordisk Investigational Site, Xi'an, Shaanxi, 710032, China|Novo Nordisk Investigational Site, Shanghai, Shanghai, 200003, China|Novo Nordisk Investigational Site, Tianjin, Tianjin, 300070, China |
URL: | https://clinicaltrials.gov/show/NCT00184561 |

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