Coronary Flow Reserve Changes After Semaglutide Treatment

NCT ID: NCT07190144

Last Updated: 2025-09-24

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

122 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-01-07

Study Completion Date

2025-08-01

Brief Summary

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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.

Detailed Description

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Conditions

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

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Non-diabetic patients

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.

No interventions assigned to this group

Diabetic patients

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

No interventions assigned to this group

Eligibility Criteria

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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
Minimum Eligible Age

28 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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MEDICANA

UNKNOWN

Sponsor Role collaborator

Ekrem Bilal Karaayvaz

OTHER

Sponsor Role lead

Responsible Party

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Ekrem Bilal Karaayvaz

Assistant Professor

Responsibility Role SPONSOR_INVESTIGATOR

Locations

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Medicana International Istanbul Hospital

Istanbul, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

References

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Marso SP, Bain SC, Consoli A, Eliaschewitz FG, Jodar E, Leiter LA, Lingvay I, Rosenstock J, Seufert J, Warren ML, Woo V, Hansen O, Holst AG, Pettersson J, Vilsboll T; SUSTAIN-6 Investigators. Semaglutide and Cardiovascular Outcomes in Patients with Type 2 Diabetes. N Engl J Med. 2016 Nov 10;375(19):1834-1844. doi: 10.1056/NEJMoa1607141. Epub 2016 Sep 15.

Reference Type BACKGROUND
PMID: 27633186 (View on PubMed)

Lincoff AM, Brown-Frandsen K, Colhoun HM, Deanfield J, Emerson SS, Esbjerg S, Hardt-Lindberg S, Hovingh GK, Kahn SE, Kushner RF, Lingvay I, Oral TK, Michelsen MM, Plutzky J, Tornoe CW, Ryan DH; SELECT Trial Investigators. Semaglutide and Cardiovascular Outcomes in Obesity without Diabetes. N Engl J Med. 2023 Dec 14;389(24):2221-2232. doi: 10.1056/NEJMoa2307563. Epub 2023 Nov 11.

Reference Type BACKGROUND
PMID: 37952131 (View on PubMed)

Other Identifiers

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IstanbulU-EBKaraayvaz-2

Identifier Type: -

Identifier Source: org_study_id

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