← Trials/Trial dossier/NCT01299012
Liraglutide as Additional Treatment in Patients With Type 1 Diabetes Mellitus
Liraglutide as Additional Treatment in Patients With Type 1 Diabetes Mellitus, a Retrospective Chart Review
Lead sponsor
Asset
Liraglutide
Subcutaneous · GLP-1 agonist
Listed sites
0
Recruiting sites
—
Enrollment
30
actual
Study population
Type 1 diabetes
Key I/E criterion
—
Primary endpoint
•Improved Blood Glucose comtrol in Type 1 Diabetes Patients with Liraglutide
Identifiers
Registered as
Timeline
Milestones
Assets
Investigational agents
Study populations
Who this study enrolls
Eligibility
Who can enroll
Study population text
Type 1 Diabetes Mellitus
Inclusion criteria
Exclusion criteria
Endpoints (1)
What's being measured
Protocol endpoints and posted registry outcome measures, grouped into outcome categories. Composite endpoints show their component event types. Standard codes (LOINC, SNOMED CT) are shown where available.
Glycemic / diabetes
1 endpointImproved Blood Glucose comtrol in Type 1 Diabetes Patients with Liraglutide
Time frame:20 weeks
descriptive, improvement
Provenance
Sources
Trial facts come from public ClinicalTrials.gov records. Endpoint categories are Delfa's classification of those records, not a ClinicalTrials.gov field. All figures reflect the July 1, 2026 snapshot.