MedPath

ADHERE-S (NIS Brilique)

Completed
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
Inclusion Criteria
  • ≥ 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
Exclusion Criteria

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
NameTimeMethod
duration (number of days) on ticagrelor therapy in patients with acute coronary syndrome1 year (12 months)
Secondary Outcome Measures
NameTimeMethod

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

© Copyright 2025. All Rights Reserved by MedPath