Injectable Semaglutide vs Dulaglutide in Individuals at Cardiovascular Risk
Completed
Conditions studied: Type 2 Diabetes Mellitus, Obesity, Overweight
In brief
Investigators are building an empirical evidence base for real world data through large-scale emulation of randomized controlled trials. The investigators' goal is to understand for what types of clinical questions real world data analyses can be conducted with confidence and how to implement such studies.
Key facts
- Study ID
- NCT07619495
- Run by
- Brigham and Women's Hospital
- People needed
- 120000
- Starts
- 2026-01-20
- Expected to finish
- 2026-06-01
- Last updated by the study team
- 2026-07-09
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Men or women aged 18 years or older
- History of myocardial infarction, stroke, any surgical or percutaneous revascularization procedure
- Use of antihypertensive or lipid-lowering drugs
- Coronary, carotid, or peripheral artery disease
- BMI greater than or equal to 25.0 mg/m2
- Type 2 diabetes
You may not qualify if…
- Medullary thyroid carcinoma
- MEN syndrome type 2
- Malignancy
- Type 1 diabetes
- Secondary diabetes
- End-stage renal disease or dialysis
- Uncontrolled diabetic retinopathy or maculopathy
- Pregnancy
- History of bariatric surgery
- Prior use of pramlintide or any GLP-1-RA, except semaglutide or dulaglutide
- Cardiovascular event or intervention in the last 7 days
Where it is running
- Brigham and Women's Hospital — Boston, Massachusetts, United States
Full record on ClinicalTrials.gov
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