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ADHERE-S (NIS Brilique)

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ClinicalTrials.gov Identifier: NCT03444012
Recruitment Status : Recruiting
First Posted : February 23, 2018
Last Update Posted : May 21, 2018
Sponsor:
Information provided by (Responsible Party):
AstraZeneca

Brief Summary:
noninterventional study investigating persistence and adherence on ticagrelor in ACS patients in Serbia

Condition or disease Intervention/treatment
ACS (Acute Coronary Syndrome) Drug: ticagrelor 90 mg

Study Type : Observational
Estimated Enrollment : 250 participants
Observational Model: Other
Time Perspective: Cross-Sectional
Official Title: Non-interventional Prospective Data Collection on Persistence and Adherence on Ticagrelor in ACS Adult Patients in Serbia
Actual Study Start Date : March 5, 2018
Estimated Primary Completion Date : June 30, 2019
Estimated Study Completion Date : June 30, 2019

Resource links provided by the National Library of Medicine

Drug Information available for: Ticagrelor


Intervention Details:
  • Drug: ticagrelor 90 mg
    persistence and adherence on ticagrelor in ACS patients


Primary Outcome Measures :
  1. duration (number of days) on ticagrelor therapy in patients with acute coronary syndrome [ Time Frame: 1 year (12 months) ]


Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Adult ACS patients
Criteria

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.


Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03444012


Contacts
Contact: Mirjana Petrovic, PhD +381113336900 mirjana.petrovic@astrazeneca.com

Locations
Serbia
Research site Recruiting
Belgrade, Serbia
Sponsors and Collaborators
AstraZeneca

Responsible Party: AstraZeneca
ClinicalTrials.gov Identifier: NCT03444012     History of Changes
Other Study ID Numbers: D5130R00052
First Posted: February 23, 2018    Key Record Dates
Last Update Posted: May 21, 2018
Last Verified: May 2018

Additional relevant MeSH terms:
Acute Coronary Syndrome
Myocardial Ischemia
Heart Diseases
Cardiovascular Diseases
Vascular Diseases
Ticagrelor
Purinergic P2Y Receptor Antagonists
Purinergic P2 Receptor Antagonists
Purinergic Antagonists
Purinergic Agents
Neurotransmitter Agents
Molecular Mechanisms of Pharmacological Action
Physiological Effects of Drugs