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Effects of visualization of successful revascularization on chest pain and quality of life

Effects of visualization of successful revascularization on chest pain and quality of life - The PLA-pCi-EBO-Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00017524
Enrollment
144
Registered
2019-07-05
Start date
2019-07-07
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

Interventions

Group 1: The patients in the intervention group receive a print out of the pictures of the procedure before and after stent implantation. Group 2: Control group: According to current clinical praxis,

Sponsors

Universitätsklinikum Regensburg
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: - symptomatic CAD (coronary artery disease) - CCS >=2 (Canadian Cardiovascular Society) - AP-frequency >=2/week - German-speaking

Exclusion criteria

Exclusion criteria: - EF <35% (ejection fraction) - severe pulmonary disease - impaired vision - impaired hearing - dementia - drugs with influence on the opiod system - high grade valve impairment - Hb <=7 mg/dL - participation in other interventional clinical trial

Design outcomes

Primary

MeasureTime frame
The Seattle Angina Questionnaire (SAQ) derived Quality of life score is assessed during the hospital stay of the angioplasty. This is repeated after 1 and 6 months in a phone interview. Primary endpoint of this study is the change in the quality of life as it is meassured in the Seattle Angina Questionnaire one and six months after stent implantation. This questionnaire is filled out by the study doctor together with the patient during the initiatl hospital stay. The follow up after 1 and 6 months is performed in a telephone interview.

Secondary

MeasureTime frame
Secondary endpoints are changes in the other derived SAQ-Scores (physical limitation, angina stability, Angina frequency, treatment satisfaction, disease perception) and the dyspnea (NYHA Score) after 1 and 6 months compared to the intial assessment during the initial hospital stay.

Countries

Germany

Contacts

Public ContactSamuel Sossalla

Universistätsklinikum Regensburg

samuel.sossalla@ukr.de09419447210

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 17, 2026