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RECRUITING
NCT05683873
NA

Stroke-induced Myocardial Dysfunction: Role of GDF-15 (SMOG-15) Clinical Work Package

Sponsor: Centre Hospitalier Universitaire Dijon

View on ClinicalTrials.gov

Summary

The aim of this study is to analyze the relationship between the blood biomarker GDF-15 and heart damage after stroke. It is being conducted in France, in the Neurology Department of the Dijon University Hospital (Burgundy). The research is interventional because a biological blood test will be performed, as well as a heart rhythm recording and several cardiac echograms during the hospitalization of the participants and during the follow-up consultation scheduled 4 to 6 months after the stroke. A total of 130 stroke patients will participate in this study. Participation includes 4 visits: * Inclusion visit (within 24 hours of the first stroke symptoms) * visit 1 (within 24 to 72 hours of stroke) * visit 2 (within 48 hours of visit 1) * Visit 3 (approximately 4-6 months post-stroke)

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

130

Start Date

2023-02-13

Completion Date

2027-08

Last Updated

2025-01-28

Healthy Volunteers

No

Conditions

Interventions

PROCEDURE

Electrocardiogram

Inclusion visit, V1, V2 and V3

PROCEDURE

transthoracic echocardiography

V1, V2 and V3

BIOLOGICAL

standard biology

Inclusion visit

BIOLOGICAL

determination of serum GDF-15, osteoprotegerin and ST-2

Inclusion visit, V1, V2 and V3

BIOLOGICAL

Ultrasensitive Troponin-Ic

Inclusion visit, V1, V2 and V3

OTHER

Collection of clinical and radiological data

Inclusion visit, V1 and V3: clinical data only V2: clinical and radiological data

OTHER

72-hour continuous Holter-ECG recording

V1

Locations (1)

Chu Dijon Bourgogne

Dijon, France