Skip to content

THE RELATİONSHİP BETWEEN BLOOD GAS PARAMETERS OBTAİNED FROM THE CORONARY SİNUS DURİNG THE PROCEDURE AND CRT RESPONSE İN PATİENTS WİTH HEART FAİLURE WHO UNDERWENT CRT IMPLANTATİON

THE RELATİONSHİP BETWEEN BLOOD GAS PARAMETERS OBTAİNED FROM THE CORONARY SİNUS DURİNG THE PROCEDURE AND CRT RESPONSE İN PATİENTS WİTH HEART FAİLURE WHO UNDERWENT CRT IMPLANTATİON

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07436377
Enrollment
65
Registered
2026-02-27
Start date
2022-09-01
Completion date
2026-03-15
Last updated
2026-02-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiac Resynchronization Therapy, Coronary Sinus, Heart Failure

Brief summary

Heart failure (HF) is one of the clinical syndromes with the highest morbidity and mortality rates among cardiovascular diseases. Despite pharmacological treatments, symptoms persist in a significant proportion of patients, and mortality cannot be prevented. Therefore, device-based therapies, particularly cardiac resynchronisation therapy (CRT), have gained an important place in the treatment algorithm.CRT aims to correct mechanical dyssynchrony by enabling simultaneous contraction of the left and right ventricles. It also aims to reduce sudden cardiac death rates with its defibrillator feature. Current guidelines emphasise that CRT provides significant benefits in terms of symptomatic improvement and long-term survival when appropriate patient selection is made. However, not all patients who meet the criteria have benefited equally from CRT. It is difficult to predict in advance which heart failure patients will benefit from CRT.The aim of the study is to analyse blood gas parameters obtained from the coronary sinus during the procedure in cases of symptomatic heart failure with low ejection fraction despite optimal medical treatment and in patients with indications for CRT according to current guidelines. This analysis aims to contribute to the prior identification of patients who may benefit.

Interventions

DIAGNOSTIC_TESTcoronary sinus blood sampling

Blood gas analysis by drawing blood from the coronary sinus

Sponsors

Trakya University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Patients diagnosed with heart failure, with an EF \<35, and in heart failure stages 2-3-4 despite optimal medical therapy. 2. Those who agree to participate in the study. 3. Patients aged 18 years and older. 4. Patients with a QRS duration of 135 ms or more on ECG.

Exclusion criteria

1. Patients with EF 35 or higher. 2. QRS duration on ECG less than 130 milliseconds. 3. Not receiving the maximum tolerable dose of medication for KY. 4. Absence of left bundle branch block morphology on ECG. 5. History of acute myocardial infarction within the last 3 months. 6. Estimated life expectancy of less than 1 year. 7. History of cardiac surgery within the last 3 months. 8. Elective cardiac surgery planned. 9. Patients scheduled for CRT prior to nodal ablation. 10. Patients with intracardiac shunts. 11. Those who refuse to participate in the study. 12. Chronic lung diseases (COPD, emphysema, bronchitis, etc.). -

Design outcomes

Primary

MeasureTime frame
Combined endpoint of hospitalization for heart failure, death, need for IV diuretics, change in ejection fraction, and change in NYHA classification6 months

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 28, 2026