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NCT03797651
Ticagrelor Monotherapy in PAtients Treated With New-generation Drug-eluting Stents for Acute Coronary Syndrome; T-PASS Trial
NA trial testing Standard DAPT in Coronary Artery Disease, Acute Coronary Syndrome in 2,850 participants. Status unknown.
4 April 2025
Quick facts
| Lead sponsor | Yonsei University |
|---|---|
| Phase | NA |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 2,850 |
| Start date | 24 April 2019 |
| Primary completion | 4 April 2025 |
| Estimated completion | 4 April 2025 |
| Sites | 1 location across South Korea |
Drugs / interventions tested
- Standard DAPT — full drug profile →
- Very-short DAPT less than 1 month after PCI — full drug profile →
Conditions studied
- Coronary Artery Disease, Acute Coronary Syndrome — all drugs for Coronary Artery Disease, Acute Coronary Syndrome →
Sponsor
Yonsei University
Who can join
Adults 19 to 80, any sex, with Coronary Artery Disease, Acute Coronary Syndrome. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
We hypothesized that ticagrelor monotherapy might be enough to prevent thromboembolic events without aspirin after PCI in patients with acute coronary syndrome(ACS). Moreover, ticagrelor monotherapy will reduce bleeding risk compared to DAPT with aspirin plus ticagrelor. We will also evaluate 1-year safety and efficacy of Orsiro stent for patient with acute coronary syndrome. After confirmation of enrollment, patients will be randomized to continue standard treatment (aspirin plus ticagrelor) for 1 year or to stop aspirin after discharge or less than 1 month after PCI (ticagrelor monotherapy). Randomization will be stratified according to 1) the presence of diabetes and 2) ST elevation myocardial infarction (MI). Baseline clinical and angiographic characteristics, laboratory findings will be assessed at the time of randomization. All patients will provide informed consent on their own initiative.
Publications & conference data
5 peer-reviewed publications reference this trial (live from Europe PMC):
-
Stopping Aspirin Within 1 Month After Stenting for Ticagrelor Monotherapy in Acute Coronary Syndrome: The T-PASS Randomized Noninferiority Trial.
Hong SJ, Lee SJ, Suh Y, Yun KH, et al · · 2024 · cited 90× · PMID 37878786 · DOI 10.1161/circulationaha.123.066943 -
Early Aspirin Discontinuation Following Acute Coronary Syndrome or Percutaneous Coronary Intervention: A Systematic Review and Meta-Analysis of Randomized Controlled Trials.
Guedeney P, Mesnier J, Sorrentino S, Abcha F, et al · · 2020 · cited 8× · PMID 32138287 · DOI 10.3390/jcm9030680 -
New pharmacological agents and novel cardiovascular pharmacotherapy strategies in 2024.
Tamargo J, Agewall S, Ambrosio G, Borghi C, et al · · 2025 · cited 6× · PMID 40058879 · DOI 10.1093/ehjcvp/pvaf012 -
Short dual antiplatelet therapy and dual antiplatelet therapy de-escalation after primary percutaneous intervention: For whom and how.
Muthspiel M, Kaufmann CC, Burger AL, Panzer B, et al · · 2022 · cited 3× · PMID 36440022 · DOI 10.3389/fcvm.2022.1008194 -
Optimal timing of aspirin discontinuation with ticagrelor monotherapy in acute coronary syndrome: a post hoc comparative analysis from the TICO and T-PASS trials.
Lee JH, Lee J, Kim SY, Jeon HS, et al · · 2026 · PMID 41697655 · DOI 10.4244/eij-d-25-00832
Verify or expand the search:
- PubMed search for NCT03797651
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT03797651 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Yonsei University
- Last refreshed: 7 March 2023
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03797651.
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