ADHERE-S (NIS Brilique)
- Conditions
- ACS (Acute Coronary Syndrome)
- Registration Number
- NCT03444012
- Lead Sponsor
- AstraZeneca
- Brief Summary
noninterventional study investigating persistence and adherence on ticagrelor in ACS patients in Serbia
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 269
- ≥ 18 years of age
- diagnosed with ACS - STEMI or NSTEMI or unstable angina, invasively or non-invasively treated
- Patients already on treatment with ticagrelor at least for 1 month and no longer than 3 months prior to study initiation. Enrolment in this study must not be trigger for ticagrelor initiation.
- read and signed the Informed Consent Form
Any contraindications as per approved SmPC of Brilique
• Patients with life-threatening conditions which could disable patients to comply with scheduled visits and/or not able to fill in the patient questionnaires.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method duration (number of days) on ticagrelor therapy in patients with acute coronary syndrome 1 year (12 months)
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (9)
CHC Bezanijska Kosa
🇷🇸Belgrade, Serbia
Institute for cardiovascular diseases, Dedinje
🇷🇸Belgrade, Serbia
CHC Zvezdara
🇷🇸Belgrade, Serbia
Medical Military Academy
🇷🇸Belgrade, Serbia
Clinical Center Kragujevac
🇷🇸Kragujevac, Serbia
CHC Zemun
🇷🇸Belgrade, Serbia
Clinical Center Nis
🇷🇸Nis, Serbia
Clinical Center of Serbia
🇷🇸Belgrade, Serbia
Institute for cardiovascular diseases of Vojvodina
🇷🇸Sremska Kamenica, Serbia