Birmingham City Hospital, Sandwell and West Birmingham NHS Trust
Birmingham, West Midlands, B18 7QH, United Kingdom
Location status: Recruiting
NCT Number: NCT06414551
A chronic total occlusion (CTO) is present in 15-20% of patients who are referred for invasive coronary angiography. CTO Percutaneous Coronary Intervention (PCI) procedure success rates have increased over the years and can be as high as 90% when performed by high-volume CTO operators.Procedurally, excess calcification in the CTO anatomy is one factor which makes it difficult to complete the procedure or obtain ideal stent expansion. Excess calcification is best identified by Computed Tomography Coronary Angiography (CTCA) rather than invasive angiography.
The investigators plan to retrospectively evaluate CTCA in patients who underwent CTO PCI and correlate calcification characteristics with CTO PCI outcomes and tools utilised for calcium modification.
Interested in participating?
Request Info18 year and older
All sexes
Observational
Birmingham, West Midlands, B18 7QH, United Kingdom
Location status: Recruiting
Cohort: All coronary CTO patients who underwent a PCI attempt and also underwent CTCA at our centre in the last 5 years.
Method of identifying and consenting patients: Screening of our local database to identify suitable patients who fulfil the inclusion/exclusion criteria. These patients will be telephoned and the consent form and participant information sheet will be maile dot them along with a self addressed stamped envelope.On receipt of the consent form, we will countersign it and return a copy to the patient. Consented patients' images and reports of the CTCA and CTO PCI will be reviewed.
Characteristics of calcification in the CTO on the CTCA will be evaluated including site, density and quantity of calcification. This will be correlated with CTO PCI outcomes of success and failure. Also this will be correlated with use of calcium modification tools for the CTO PCI.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: up to 24 hours
Success or failure
Time frame: up to 24 hours
Percentage of patients in whom any calcium modifying tool was used and the corelation of this with the severity of calcification.
Contact information is provided by the study sponsor or research team.
Kelly Hard
CONTACT
Vinoda Sharma, FRCP
CONTACT
Sandwell & West Birmingham Hospitals NHS Trust
Other
Characteristics of Calcification in a Chronic Total Occlusion on Computed Tomography Coronary Angiogram and Percutaneous Coronary Intervention Outcomes- a Single Centre Observational Study
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT03756870
Cardiovascular Diseases, Chronic Total Occlusion of Coronary Artery
Amsterdam, Netherlands
View Trial DetailsNCT03667196
Chronic Total Occlusion of Coronary Artery
Anyang, South Korea
View Trial DetailsNCT03563417
Cardiovascular Diseases, Chronic Total Occlusion of Coronary Artery
Aarhus N, Denmark
View Trial DetailsNCT06193954
Chronic Angina, Chronic Total Occlusion of Coronary Artery
Atlanta, Georgia, United States
View Trial Details