Last reviewed · How we verify
NCT04977076: SLIM-2
Comparison Between Direct Oral Anticoagulation (DOAC) Interruption and DOAC Continuation in Patients Undergoing Elective Invasive Coronary Angiography or Percutaneous Coronary Intervention
NA trial testing Uninterrupted NOAC use in Atrial Fibrillation in 1,214 participants. Status unknown.
31 December 2023
Quick facts
| Lead sponsor | Zuyderland Medisch Centrum |
|---|---|
| Phase | NA |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | prevention |
| Enrollment | 1,214 |
| Start date | 1 October 2021 |
| Primary completion | 31 December 2023 |
| Estimated completion | 31 December 2023 |
Drugs / interventions tested
- Uninterrupted NOAC use
- Interrupted NOAC use
Conditions studied
- Atrial Fibrillation — all drugs for Atrial Fibrillation →
- Coronary Artery Disease — all drugs for Coronary Artery Disease →
- Anticoagulants — all drugs for Anticoagulants →
Sponsor
Zuyderland Medisch Centrum — full company profile →
Who can join
18 and older, any sex, with Atrial Fibrillation or Coronary Artery Disease. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
A prospective, multicenter, 1:1 randomized, investigator initiated study. Goal of this study is to examine the safety of uninterrupted periprocedural NOAC use.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Direct oral anticoagulation interruption vs continuation in patients undergoing elective invasive coronary angiography or percutaneous coronary intervention: Design and rationale of the South Limburg Myocardial Infarction Study Group Trial 2 (SLIM-2).
Janssen S, Luijkx JJP, Swinnen W, Vriesendorp P, et al · · 2026 · PMID 42055156 · DOI 10.1016/j.ahj.2026.107462
Verify or expand the search:
- PubMed search for NCT04977076
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other Zuyderland Medisch Centrum trials
Trials by the same sponsor.
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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 NCT04977076 (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 Zuyderland Medisch Centrum
- Last refreshed: 26 July 2021
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/NCT04977076.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing