Actively Recruiting
Systematic Post-Implementation Evaluation of Stents
Led by Vastra Gotaland Region · Updated on 2023-04-27
6000
Participants Needed
1
Research Sites
185 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
To conduct a quality assurance project to establish the differences in health care processes and cost effectiveness of having the thin-strut Orsiro stent versus the thicker strut Promus stent on the shelf (i.e. as the most accessible stent).
CONDITIONS
Official Title
Systematic Post-Implementation Evaluation of Stents
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients undergoing PCI at any hospital participating in the study
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Kardiologen
Gothenburg, Sweden, 41345
Actively Recruiting
Research Team
B
Björn Redfors, MD, PhD
CONTACT
O
Oskar Angerås, MD, PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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