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NCT05592535

Outcomes With Fractional Flow Reserve in Chronic Coronary Syndrome

Completed Last updated 24 October 2022
What this trial tests

trial testing Coronary revascularization in Chronic Coronary Syndrome in 5,000 participants. Completed in 1 June 2020.

Timeline
1 June 2015
Primary endpoint
1 June 2020
1 June 2020

Quick facts

Lead sponsorUppsala University
StatusCompleted
Study typeOBSERVATIONAL
Enrollment5,000
Start date1 June 2015
Primary completion1 June 2020
Estimated completion1 June 2020

Drugs / interventions tested

Conditions studied

Sponsor

Uppsala University

Who can join

Eligibility, any sex, with Chronic Coronary Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The use of fractional flow reserve (FFR) to assess the functional relevance of coronary stenoses has been demonstrated to reduce the risk urgent revascularization in chronic coronary syndrome patients.\[1\] The goal of this study is to assess whether the utility of using FFR during percutaneous coronary intervention (PCI) in chronic coronary syndrome patients is confirmed in a real-life scenario. This study will implement a regression discontinuity design (RDD). RDD is a quasi-experimental study design able to provide robust findings on causality using observational data.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Chronic Coronary Syndrome

Currently open trials in the same condition.

Other Uppsala University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05592535.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing