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NCT07204847Completed

Prognostic Impact of Guideline-recommended Timing for Invasive Strategy in NSTEMI

Prognostic Impact of Guideline-recommended Timing for Invasive Strategy in NSTEMI: a Prospective Real-world Study

Source: ClinicalTrials.gov · Last updated 2 Oct 2025

Brief summary (registry, in English)

The objective of this multicentric observational study is to evaluate the prognostic influence of adherence or non-adherence to the recommended coronary angiography timeframe (within 24 hours) and the six-month prognosis of the patients.

Status (registry)
Completed
Study type
Observational
Enrollment
407 (actual)
First submitted
15 Sept 2025
Start date
1 Nov 2023
Primary completion date
1 May 2025
Lead sponsor
University Hospital, Montpellier
NCT number
NCT07204847

What you commit to

  • Study type: Observational
  • Participants enrolled: 407
  • From 1 Nov 2023 to the primary completion date, 1 May 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • STEMI (ST-segment elevation myocardial infarction) or equivalent (defined as chest pain with ECG changes and troponin elevation \> 5 times the normal with an occluded artery (TIMI 0, 1, or 2) during initial coronary angiography)
  • Very high-risk NSTEMI (hemodynamic instability, cardiogenic shock, recurrent/refractory chest pain despite optimal medical treatment, life-threatening arrhythmia, mechanical complication, heart failure clearly related to NSTEMI, ST depression \> 1mm/6 leads with ST elevation in aVR and/or V1) for which urgent coronary angiography is mandatory
  • Unstable angina (acute coronary syndrome without troponin elevation)
  • Recovered cardiac arrest
  • Other diagnoses considered after coronary angiography (e.g., myocarditis, Takotsubo syndrome)

Age

  • Age \< 18 years

Other

  • Troponin elevation without chest pain or symptoms suggestive of NSTEMI
  • Contraindication to coronary revascularization or coronary angiography

Who the study is looking for

  • Presence of chest pain with or without ECG changes
  • Elevation of troponin level \> 90th percentile or a significant increase between two dosages
  • Significant or non-significant coronary lesion confirming the diagnosis of coronary artery disease on coronary angiography (coronary angiography mandatory before inclusion to confirm NSTEMI)

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
CHU de Montpellier
Coordinator of this site? Confirm its status
MontpellierFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.