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Active not recruitingPhase NA

The Effect of Combined Dulaglutide and Dapagliflozin Treatment vs DPP-4 Inhibitors in Endothelial and Vascular Function in Patients With Type 2 Diabetes Mellitus and Albuminuria

Study of Endothelial Glycocalyx and Vascular Function in Patients With Type 2 Diabetes and Albuminuria After Administration of Dulaglutide and Dapagliflozin vs DPP-4 Inhibitors

Lead sponsor

Attikon Hospital

Asset

Dulaglutide

Subcutaneous · GLP-1 agonist

Listed sites

1

Recruiting sites

Enrollment

60

actual

Study population

Chronic kidney disease, Type 2 diabetes

Key I/E criterion

HbA1c 7-10%

Primary endpoints

UACR, changePWVPBR

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

NCT IDNCT06611904
Org study ID456/11-06-2017

Timeline

Milestones

Study start2018-02-01actual
Primary completion2022-02-05actual
Study first posted2024-09-25actual
Last update posted2024-09-25actual
Study completion2024-12-15estimated

Assets

Investigational agents

Study populations

Who this study enrolls

Chronic kidney diseaseType 2 diabetes

Eligibility

Who can enroll

Minimum age18 Years
Maximum age80 Years
SexAll
Healthy volunteersNot accepted

Inclusion criteria

Type 2 diabetes mellitus Albuminuria HbA1c: 7-10% eGFR\> 60 ml/min

Exclusion criteria

Type 1 diabetes mellitus Inflammation, chronic or acute Established cardiovascular disease Malignancy within the last 5 years

Endpoints (4)

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

Other (unclassified)
2
Renal / kidney
1
Cardiometabolic biomarkers
1

Renal / kidney

1 endpoint
Primary/protocol endpoint

UACR

Time frame:4 and 12 months

uACR, change

ratio, improvement

LOINC 9318-7

Cardiometabolic biomarkers

1 endpoint
Primary/protocol endpoint

PWV

Time frame:4 and 12 months

change from baseline, improvement

Other (unclassified)

2 endpoints
Primary/protocol endpoint/low confidence

PBR

Time frame:4 and 12 months

change from baseline, descriptive

Primary/protocol endpoint/low confidence

GLS

Time frame:4 and 12 months

change from baseline, improvement

Publications (3)

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.

Provenance

Sources

Trial identity, design, statusClinicalTrials.gov API v2
Snapshot dateJuly 1, 2026
Endpoint classificationDelfa endpoint taxonomy v2 (May 13, 2026)
Results tableno registry results posted yet

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.