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NCT07088718Completed

Prediction of the SURPASS-CVOT Cardiovascular Outcome Trial in Healthcare Claims Data

Source: ClinicalTrials.gov · Last updated 15 Oct 2025

Brief summary (registry, in English)

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.

Status (registry)
Completed
Study type
Observational
Enrollment
44671 (actual)
First submitted
19 Jul 2025
Start date
1 Oct 2024
Primary completion date
30 Jul 2025
Lead sponsor
Brigham and Women's Hospital
NCT number
NCT07088718

What you commit to

  • Study type: Observational
  • Participants enrolled: 44671
  • From 1 Oct 2024 to the primary completion date, 30 Jul 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior use of pramlintide or any GLP-1-RA except tirzepatide or dulaglutide
  • Concurrent use of both drugs i.e. tirzepatide and dulaglutide

Other illness

  • Medullary thyroid carcinoma, MEN syndrome type 2, malignancy
  • Treatment for diabetic retinopathy//macular edema, pancreatitis, gastric emptying abnormality/bariatric surgery, liver disease, end-stage renal disease or dialysis, pregnancy
  • Cardiovascular event, hospitalization for heart failure

Who the study is looking for

  • History of MI, surgical or percutaneous coronary/carotid peripheral artery revascularization
  • BMI ≥25.0kg/m2
  • Type 2 diabetes, diagnosis of coronary/carotid/peripheral artery disease
  • Age ≥40 years
  • Male or female sex

Criteria the registry did not label

  • FOLLOWING ELIGIBILITY CIRTERIA OF THE SURPASS-CVOT TRIAL

Age in the registry: 40 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Brigham and Women's Hospital
Coordinator of this site? Confirm its status
BostonUnited StatesUnknown status

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.