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Dulaglutide in Diabetic Patients, Relationship Between Arterial Stiffness, Endothelial Function, Clinical and Laboratory Variables
Arterial Stiffness and Endothelial Function Indexes, Relationships With Clinical and Laboratory Variables in a Group of Diabetic Patients in Treatment With Dulaglutide: a Case-control Study
Lead sponsor
Asset
Dulaglutide
Subcutaneous · GLP-1 agonist
Listed sites
1
Recruiting sites
—
Enrollment
92
actual
Study population
Type 2 diabetes
Key I/E criterion
—
Primary endpoint
•Change from Baseline Reactive Hyperemia Index at 3 and 9 months
Footprint
Where this trial recruits
Site locations as reported to ClinicalTrials.gov. Site count is not enrollment count; per-site enrollment is not available from source.
Identifiers
Registered as
Timeline
Milestones
Assets
Investigational agents
Study populations
Who this study enrolls
Eligibility
Who can enroll
Inclusion criteria
Exclusion criteria
Endpoints (8)
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.
Coverage by outcome category
Weight & body composition
1 endpointChange from Baseline Body Mass Index at 3 and 9 months
Time frame:0 months, 3 months and 9 months
BMI, change
change from baseline, improvement
Glycemic / diabetes
1 endpointChange from Baseline glucose at 3 and 9 months
Time frame:0 months, 3 months and 9 months
Fasting glucose, change
change from baseline, improvement
LOINC 1558-6
Cardiometabolic biomarkers
5 endpointsChange from Baseline systolic blood pressure at 3 and 9 months
Time frame:0 months, 3 months and 9 months
Systolic BP, change
change from baseline, improvement
LOINC 8480-6
Change from Baseline cholesterol at 3 and 9 months
Time frame:0 months, 3 months and 9 months
Total cholesterol, change
change from baseline, improvement
LOINC 2093-3
Change from Baseline triglycerides at 3 and 9 months
Time frame:0 months, 3 months and 9 months
Triglycerides, change
change from baseline, improvement
LOINC 2571-8
Change from Baseline diastolic blood pressure at 3 and 9 months
Time frame:0 months, 3 months and 9 months
Diastolic BP, change
change from baseline, improvement
LOINC 8462-4
Change from Baseline Pulse Wave Velocity at 3 and 9 months
Time frame:0 months, 3 months and 9 months
change from baseline, improvement
Other (unclassified)
1 endpointChange from Baseline Reactive Hyperemia Index at 3 and 9 months
Time frame:0 months, 3 months and 9 months
change from baseline, improvement
Publications (1)
Bibliography
Records linked to this trial through ClinicalTrials.gov references, PubMed NCT search, and curated study seeds. 'Canonical' marks design/result papers; others are registry references or candidates.
Registry references + supporting bibliography
- The Cochrane database of systematic reviews2025 Feb 18PMID39963952doi:10.1002/14651858.CD015849.pub2via clinicaltrials gov reference derived + pubmed nct search
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.