Trials / Completed
CompletedNCT03888157
A Research Study Looking at How Victoza® Works in People With Type 2 Diabetes in Iran, Followed in Local Clinical Routine
A Multi-centre, Prospective, Non-interventional Study Investigating the Effect of Victoza® in Patients With Type 2 Diabetes in Iran Followed in a Real World Setting
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 839 (actual)
- Sponsor
- Novo Nordisk A/S · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- —
Summary
The purpose of the study is to collect information on how the medicine Victoza® (liraglutide) works in people with Type 2 diabetes in Iran. Patients will get Victoza® as prescribed to them by their study doctor. The study will last for about 5 to 8 months. Patients will be asked to complete some questionnaires about their health and diabetes treatment. Patients will complete these during their normally scheduled visits with study doctor.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Liraglutide | Patients will be treated according to the Iranian label for Victoza®, following routine clinical practice and at the discretion of the study doctor. The study doctor will determine the intended maintenance dose of Victoza®, as well as any changes to the maintenance dose thereafter. Patients will be treated according to the Iranian label for Victoza®, following routine clinical practice and at the discretion of the study doctor. The study doctor will determine the intended maintenance dose of Victoza®, as well as any changes to the maintenance dose thereafter. The physician's decision to initiate treatment with Victoza® is clearly separate from the opportunity to include the patient in the study. |
Timeline
- Start date
- 2019-03-10
- Primary completion
- 2020-10-21
- Completion
- 2020-10-21
- First posted
- 2019-03-25
- Last updated
- 2021-07-14
Locations
16 sites across 1 country: Iran
Source: ClinicalTrials.gov record NCT03888157. Inclusion in this directory is not an endorsement.