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Coronary Flow Reserve Changes After Semaglutide Treatment

E

Ekrem Bilal Karaayvaz

Status

Completed

Conditions

Obesity &Amp; Overweight
The Study Focused on the Vascular Effects of Semaglutide in Both Diabetic and Non-diabetic Patients

Study type

Observational

Funder types

Other

Identifiers

NCT07190144
IstanbulU-EBKaraayvaz-2

Details and patient eligibility

About

The goal of this observational study is to learn about the effects of semaglutide to coronary artery flow in diabetic and non-diabetic patients. The main question it aims to answer is:

Does semaglutide enhance coronary artery flow in diabetic and non-diabetic patients?

Participants already planned taking semaglutide by an endocrine specialist as their treatment was assessed with CFR before and 3 months after.

Enrollment

122 patients

Sex

All

Ages

28 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients who were planned to start semaglutide.

Exclusion criteria

  • Ischemic heart disease
  • Previous stent implantation or coronary bypass
  • Heart failure
  • Cardiomyopathies
  • Inflammatory diseases
  • Autoimmune rheumatic disease
  • Chronic liver and renal insufficiency

Trial design

122 participants in 2 patient groups

Non-diabetic patients
Description:
Non-diabetic patients who have planned to given semaglutide by an endocrinology specialist, mostly to give weight, were performed CFR with echocardiography before and 3 months after the treatment.
Diabetic patients
Description:
Diabetic patients, who were planned to start semaglutide by an endocrinology specialist and were otherwise has same demographic data as non-diabetic patients, were performed CFR with echocardiography before and 3 months after the treatment

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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