Patient Reported Outcome in Bioresorbable Vascular Scaffold

Patient Reported Outcome in Bioresorbable Vascular Scaffold - PRO_BVS

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00007398

Enrollment

150

Registered

2014-11-11

Start date

2014-11-15

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

I25.1

Interventions

Group 1: Assessment of Health Related Quality of Life, Mental Distress and Illness perception in patients with Coronary Artery disease after PCI with bioresorbable vascular scaffold

Eligibility

Sex/Gender

All

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Coronary Artery disease and Implantation of bioresorbable vascular Absorb scaffold

Exclusion criteria

Exclusion criteria: acute myocardial infarction, percutaneus coronary intervention <6 months before inclusion, insufficient German language skills to answer questionnaires

Design outcomes

Primary

Measure	Time frame
Changes of MacNew Health Related Quality of Life after 1,6,12 and 24 month after PCI	—

Secondary

Measure	Time frame
Changes in HADS Mental Distress and BIPQ illness perception 1,6,12 and 24 months after PCI	—

Countries

Austria, Germany

Contacts

Public ContactOliver Friedrich

Karl Landsteiner Institut für Wissenschaftliche Forschung inder Klinischen Kardiologie

o.friedrich@karl-landsteiner.at+ 43 1 910 21-85211

Outcome results

None listed

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