Acute Coronary Syndrome (ACS) Clinical Trial
Official title:
Real-TICA Real Life Long-term Adherence to Ticagrelor After PCI for Acute Coronary Syndromes. Evaluation of Antiplatelet Therapy After 12 Months in Patients Undergoing PCI and Treated With Ticagrelor During the Acute Phase of an ACS.
Documentation of long-term data regarding ticagrelor use and evaluation of reasons for discontinuation of ticagrelor in patients with ACS
REAL-TICA is a retrospective non-interventional study to assess the long-term use of
ticagrelor in patients with ACS and to evaluate the reasons for discontinuation of
ticagrelor.
For this purpose, selected sites from the ALKK-PCI registry and the respective patients will
be identified. The sites' eligibility for this study includes the frequent use of ticagrelor
during the acute phase of ACS. Eligible patients are characterised by the diagnosis of ACS
and the use of ticagrelor during PCI.
The eligible sites will be contacted by IHF and asked to contact their eligible patients by
letter to obtain informed consent of the patients for the planned 12M follow-up by IHF. A
detailed questionnaire on events within the last 12 months, current symptoms, current
medication and the use of ticagrelor will be added to the patients' letters. Patients then
are asked to return their responses on consent to participate in the study as well as the
filled in questionnaire to IHF. Alternatively, patients may choose to receive a telephone
call by IHF to answer the detailed questionnaire in person. In case of essential information
missing, IHF will contact the primary care physician of the patient directly to obtain
information about clinical events and medications.
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