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Observational Study on Efficacy and Safety of Liraglutide in Subjects With Type 2 Diabetes

Conditions for Prescribing Liraglutide in Medical Practice and Assessment of Maintenance Level, Tolerability, and Efficacy of Victoza® (Liraglutide) in Subjects With Type 2 Diabetes

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01226966
Acronym
EVIDENCE
Enrollment
3152
Registered
2010-10-22
Start date
2010-09-30
Completion date
2013-11-30
Last updated
2017-02-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetes, Diabetes Mellitus, Type 2

Brief summary

This observational study is conducted in Europe. The aim of this non-interventional (observational) study is to evaluate the efficacy of liraglutide (Victoza®) and to assess the conditions of use of Victoza® in daily medical practice in France.

Interventions

DRUGliraglutide

Prescription is done at the discretion of the prescribing physician as part of normal clinical routine.

Sponsors

Novo Nordisk A/S
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients diagnosed with type 2 diabetes * Patients having recently started (for less than one week) or starting liraglutide (Victoza®) treatment

Exclusion criteria

* Hypersensitivity (allergy) to liraglutide or to any of the excipients * Patient is participating in a clinical trial at the inclusion * Type 1 diabetes

Design outcomes

Primary

MeasureTime frame
Percentage of patients still in liraglutide treatment and having a HbA1c (glycosylated haemoglobin) value below 7.0%Month 24

Secondary

MeasureTime frame
Change in HbA1c at month 3Month 0, Month 3
Change in HbA1c at month 6Month 0, Month 6
Change in HbA1c at month 12Month 0, Month 12
Change in HbA1c at month 18Month 0, Month 18
Change in HbA1c at month 24Month 0, Month 24
Change in fasting plasma glucose (FPG) at month 3Month 0, Month 3
Change in fasting plasma glucose (FPG) at month 6Month 0, Month 6
Change in fasting plasma glucose (FPG) at month 12Month 0, Month 12
Change in fasting plasma glucose (FPG) at month 18Month 0, Month 18
Change in fasting plasma glucose (FPG) at month 24Month 0, Month 24
Change in Body Weight at Month 3Month 0, Month 3
Change in Body Weight at Month 6Month 0, Month 6
Change in Body Weight at Month 12Month 0, Month 12
Change in Body Weight at Month 18Month 0, Month 18
Change in Body Weight at Month 24Month 0, Month 24

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 15, 2026