TADCLOT- a Double Blind Randomized Controlled Trial
Pakistan2,200 participantsStarted 2024-02-19
Plain-language summary
Compare the safety and efficacy of a twice-daily Clopidogrel regimen vs. Ticagrelor in reducing major adverse events in patients undergoing primary PCI in a double-blind randomized controlled trial.
Who can participate
Age range18 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* ST-segment elevation ≥1 mm in ≥ 2 contiguous ECG leads or New or presumably New left bundle branch block
* Age ≥18 years
* Written informed consent
Exclusion Criteria:
* Patients with STEMI secondary to stent thrombosis or index event being a complication of PCI within 30 days
* Thrombolytic therapy \<24 hours
* Platelet count \< 100,000 and Hemoglobin \<10 gm/dl
* Pregnancy or lactation
* Moderate to severe hepatic impairment
* Patients with advanced CKD and those on hemodialysis
* Recent ICH or major bleed requiring transfusion
* Inability to give informed consent
* Participation in another study
* Inability to fulfill protocol (living outside the city etc.)
What they're measuring
1
Evaluation of efficacy and safety
Timeframe: 30 days
Trial details
NCT IDNCT06318481
SponsorNational Institute of Cardiovascular Diseases, Pakistan