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GLP-1REWIN

Unknown

GLP-1 REceptor Agonists and Real World EvIdeNce

Effectiveness and Persistence of Therapy With GLP-1 Receptor Agonists in Clinical Practice. A Multicenter Retrospective Study

Assets

Dulaglutide / Exenatide / Liraglutide / Lixisenatide

Listed sites

6

Recruiting sites

Enrollment

6,000

estimated

Study population

Type 2 diabetes

Key I/E criterion

Primary endpoint

HbA1c, change

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 IDNCT03959865
Org study ID4462/AO/18

Timeline

Milestones

Study start2018-12-19actual
Primary completion2019-02-11actual
Study first posted2019-05-22actual
Last update posted2019-05-22actual
Study completion2019-05-31estimated

Assets

Investigational agents

Study populations

Who this study enrolls

Type 2 diabetes

Eligibility

Who can enroll

Minimum age18 Years
Maximum age80 Years
SexAll
Sampling methodNon probability sample

Study population text

Type 2 diabetic patients attending diabetes specialist clinics in North East Italy.

Inclusion criteria

Type 2 diabetes
Diabetes duration of at least 1 year
Initiated on a GLP-1RA during the data collection period

Exclusion criteria

Type 1 diabetes
Previous therapy with a GLP-1RA before the data collection period

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

Weight & body composition
1
Glycemic / diabetes
1
Cardiometabolic biomarkers
1
Safety / tolerability / PK
1

Weight & body composition

1 endpoint
Secondary/protocol endpoint

Weight

Time frame:3-12 months

Body weight, absolute change (kg)

change from baseline, improvement

Glycemic / diabetes

1 endpoint
Primary/protocol endpoint

HbA1c

Time frame:3-12 months

HbA1c, change

change from baseline, improvement

LOINC 4548-4

Cardiometabolic biomarkers

1 endpoint
Secondary/protocol endpoint

Blood pressure

Time frame:3-12 months

Systolic BP, change

change from baseline, improvement

LOINC 8480-6

Safety / tolerability / PK

1 endpoint
Secondary/protocol endpoint

Persistence

Time frame:3-12 months

threshold achievement, descriptive

Publications (6)

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

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.