Trials / Unknown
UnknownNCT04567290
Pharmacodynamic Evaluation of Antiplatelet Effect of Swallowing Versus Chewing Ticagrelor in Patients With Acute Coronary Syndrome
- Status
- Unknown
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 50 (estimated)
- Sponsor
- Centro Hospitalario La Concepcion · Academic / Other
- Sex
- All
- Age
- 19 Years – 85 Years
- Healthy volunteers
- Not accepted
Summary
The study aims to determine the pharmacodynamic performance in the first hour measured with verifynow, of the conventional ticagrelor loaded dose versus chewed ticagrelor in patients with acute coronary syndrome treated with percutaneous coronary intervention
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Chewed ticagrelor | Chewed ticagrelor (Brilinta) 90 mg tablets, 2 tablets |
| DRUG | Swallowed ticagrelor | Swallowed ticagrelor (Brilinta) 90 mg tablets, 2 tablets |
Timeline
- Start date
- 2020-10-07
- Primary completion
- 2021-08-15
- Completion
- 2021-09-30
- First posted
- 2020-09-28
- Last updated
- 2021-07-29
Locations
1 site across 1 country: Mexico
Source: ClinicalTrials.gov record NCT04567290. Inclusion in this directory is not an endorsement.