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Bioresorbable vascular scaffolds in ST-elevation myocardial infarction – OCT-guided implantation and mid-term OCT resultsd

Bioresorbable vascular scaffolds in ST-elevation myocardial infarction – OCT-guided implantation and mid-term OCT resultsd - DESolve-STEMI-OCT

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
DRKS
Registry ID
DRKS00009788
Enrollment
50
Registered
2015-12-15
Start date
2016-03-22
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

I21

Interventions

Group 1: STEMI DESolve (bioresorbable vascular scaffolds (BRS) in Patient with ST-Segment myocardial Infarction (STEMI). Every Patient with STEMI and BRS is enrolled in the study. Additional the Patie

Sponsors

Universitätsklinikum Bonn
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: -All Patients with STEMI and with a anatomically suitable coronarstatus -Written agreement of the Patient

Exclusion criteria

Exclusion criteria: -Intellectual reduction, No suitable coronarstatus (ostial leasion, bifurcation, calc rich leasions)

Design outcomes

Secondary

MeasureTime frame
-TIMI 0, I, II, III Fluss -Angina Pectoris -Successfull Stent-Implantationen -Target vessel failure (cardiac death, target vessel MI, or clinically driven target vessel revascularisation (TVR), and scaffold thrombosis (ST)) -Kidneyinjury -Rhythm-Events

Primary

MeasureTime frame
device-oriented composite endpoint within 36 Month (target lesion failure [TLF]), defined as the combination of cardiac death, target vessel MI, or clinically driven target lesion revascularisation (TLR), either percutaneous or surgical. Deaths that could not be attributed to another cause were re-garded as cardiac deaths. OCT subgroup: neointima formation after 4-6 month

Countries

Germany

Contacts

Public ContactFelix Hauptmann

Brüderkrankenhaus Trier

f.hauptmann@bk-trier.de01736400438

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026