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Clinical Trials/NCT07002164
NCT07002164RecruitingNot Applicable

Trial of IMmediate Invasive Versus Delayed Coronary ANGiography in Non-ST-Segment Elevation Myocardial Infarction Complicated by Acute Decompensated Heart Failure: The TIMING-AHF Trial

Chonnam National University Hospital20 sites in 1 country780 target enrollmentStarted: July 15, 2025Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
780
Locations
20
Primary Endpoint
A cumulative incidence rate of all-cause death, non-fatal myocardial infarction (MI), or hospitalization for heart failure (HF)

Study Overview

Brief Summary

Study objectives:

To determine the optimal timing of coronary angiography (CAG) in patients with non-ST-segment elevation myocardial infarction (NSTEMI) complicated by acute decompensated heart failure (AHF). The primary objective of this trial is to test the hypothesis that immediate CAG ≤2 hours after establishment of NSTEMI diagnosis would result in a significant reduction in primary composite outcome of death from any cause, non-fatal myocardial infarction (MI), or hospitalization for heart failure (HF) at 12 months after randomization as compared with delayed CAG after stabilization.

Study hypothesis:

Immediate CAG ≤2 hours after establishment of NSTEMI diagnosis would result in a significant reduction in primary composite outcome of death from any cause, non-fatal myocardial infarction (MI), or hospitalization for heart failure (HF) at 12 months after randomization as compared with delayed CAG after stabilization.

Background:

Although current guidelines recommend early CAG within 2 hours for patients with NSTEMI complicated by AHF, many patients with NSTEMI complicated by AHF did not receive early CAG. However, no randomized clinical trials have evaluated the optimal timing of CAG in patients with NSTEMI complicated by AHF. Therefore, the investigators aimed to perform a prospective, investigator-initiated, open-label, muilticenter trial to compare the efficacy and safety between immediate CAG (CAG <2 hours after establishment of NSTEMI diagnosis) and delayed CAG after stabilization (i.e. improved dyspnea and disappearance of pulmonary congestion) in participants with NSTEMI complicated by AHF.

Study procedure:

Following the establishment of NSTEMI diagnosis, participants fulfilling the eligibility criteria will be randomized at a ratio of 1:1 to immediate CAG ≤2 hours after randomization or delayed CAG after stabilization on another day during hospitalization.

Detailed Description

Acute decompensated heart failure (AHF) is frequently encountered in patients with non-ST-segment elevation myocardial infarction (NSTEMI), and it is known to be associated with worse clinical outcomes that those without heart failure (HF). Although current guidelines recommend immediate invasive strategy for patients with NSTEMI complicated by AHF, its evidence is lack. It is difficult to decide whether to perform early coronary angiography (CAG) according to the guidelines in these high-risk patients due to the risk of procedural complications. Furthermore, the most of randomized trials regarding the timing of CAG in non-ST-segment elevation acute coronary syndrome (NSTE-ACS) have excluded these patients, therefore, there is lack of evidence for performing immediate CAG in such cases. In clinical practice, many patients with NSTEMI complicated by AHF did not receive early CAG. There are only two observational studies which investigated this issue. In the Korean nationwide registry data, a total of 1,027 patients with NSTEMI complicated by AHF were analyzed, and 14.5% among study population underwent early CAG within 2 hours according to the guidelines. All-cause mortality at 12 months was not significantly different irrespective of CAG timing. In other single-center study, early CAG <24 hours was associated with a lower risk of adverse cardiac outcomes compared with delayed CAG ≥24 hours after admission.

Several studies have demonstrated improved clinical outcomes in high-risk patients with NSTE-ACS undergoing early CAG, whereas others have found no significant differences in clinical outcomes. Randomized clinical trials, such as SISCA, ISAR-COOL, RIDDLE-NSTEMI and EARLY, have demonstrated the advantages of early CAG compared to delayed invasive approach (i.e. CAG after stabilization) in high-risk patients with NSTE-ACS. The other trials regarding this issue have failed to show the superiority of early CAG over delayed invasive approach. However, no randomized clinical trials have evaluated the optimal timing of CAG in patients with NSTEMI complicated by AHF.

Therefore, the investigators aimed to perform a prospective, investigator-initiated, open-label, muilticenter trial to compare the efficacy and safety between immediate CAG (CAG <2 hours after establishment of NSTEMI diagnosis) and delayed CAG after stabilization (i.e. improved dyspnea and disappearance of pulmonary congestion) in participants with NSTEMI complicated by AHF.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
19 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Age ≥19 years
  • •Non-ST-segment elevation myocardial infarction
  • •New-onset or worsening of dyspnea (New York Heart Association class ≥2)
  • •Pulmonary congestion
  • •Patient's or guardian's consent after understanding the study

Exclusion Criteria

  • •Cardiogenic shock at initial presentation
  • •ST-segment elevation myocardial infarction
  • •ST-segment elevation ≥0.1 mV in at least 2 contiguous leads, or
  • •New onset left bundle branch block
  • •Posterior wall myocardial infarction
  • •Refractory angina
  • •Life threatening ventricular arrhythmias
  • •Life expectancy <1 year
  • •Apparently non-ischemic cause of HF
  • •Pregnancy and lactation
  • •History of coronary artery bypass grafting (CABG), or planned CABG
  • •Patient's refusal to participate in study

Arms & Interventions

Immediate coronary angiography within 2 hours after diagnosis of non-ST-segment elevation myocardial

Experimental

Coronary angiography will be performed within 2 hours after diagnosis of non-ST-segment elevation myocardial infarction.

Intervention: Immediate coronary angiography (Procedure)

Delayed coronary angiography after stabilization of acute decompensated heart failure

Active Comparator

Coronary angiography will be performed after disappearance of symptoms and signs of acute decompensated heart failure.

Intervention: Delayed coronary angiography (Procedure)

Outcomes

Primary Outcomes

A cumulative incidence rate of all-cause death, non-fatal myocardial infarction (MI), or hospitalization for heart failure (HF)

Time Frame: 1 year

Secondary Outcomes

  • A cumulative incidence rate of all-cause death, non-fatal MI, or hospitalization for HF(1, 6, 24, 36 months)
  • All-cause death(1, 6, 12, 24, 36 months)
  • Non-fatal MI(1, 6, 12, 24, 36 months)
  • Hospitalization for HF(1, 6, 12, 24, 36 months)
  • Cardiovascular death(1, 6, 12, 24, 36 months)
  • Recurrent ischemia(1, 6, 12, 24, 36 months)
  • All unplanned revascularization(1, 6, 12, 24, 36 months)
  • Definite or probable stent thrombosis(1, 6, 12, 24, 36 months)
  • Stroke(1, 6, 12, 24, 36 months)
  • Major bleeding by Bleeding Academic Research Consortium(1, 6, 12, 24, 36 months)
  • Acute kidney injury (AKI) and AKI requiring renal replacement therapy(Up to 7 days)
  • In-hospital death rate from any cause(Up to 30 days)
  • In-hospital death rate from cardiovascular cause(Up to 30 days)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Min Chul Kim

Professor

Chonnam National University Hospital

Study Sites (20)

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