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NCT05721170: BETA-TAVI
Impact of Beta Blockers on TAVI (BETA-TAVI)
Phase 4 trial testing Beta blocker in Aortic Valve Stenosis in 347 participants. Currently enrolling.
30 January 2028
Quick facts
| Lead sponsor | National and Kapodistrian University of Athens |
|---|---|
| Phase | Phase 4 |
| Status | Recruiting now |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 347 |
| Start date | 1 June 2024 |
| Primary completion | 30 January 2028 |
| Estimated completion | 31 January 2028 |
| Sites | 2 locations across Greece, Cyprus |
Drugs / interventions tested
- Beta blocker — full drug profile →
Conditions studied
- Aortic Valve Stenosis — all drugs for Aortic Valve Stenosis →
Sponsor
National and Kapodistrian University of Athens
Who can join
18 and older, any sex, with Aortic Valve Stenosis. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This is a prospective, multicentre, investigator-initiated, randomized clinical trial clinical trial investigating the impact of beta-blockers administration among patients undergoing TAVI for severe aortic valve stenosis. Adults already receiving beta-blockers be assigned randomly in 1:1 ratio to either continue or withdraw the beta-blockers medication at least 72 hours before and at least 7 days after TAVI. The primary endpoint is permanent pacemaker implantation rates in 7 days after the procedure. Secondary endpoints include death, cardiogenic shock and arrhythmias/conduction abmormalities with time frame 12 months.
Publications & conference data
2 peer-reviewed publications reference this trial (live from Europe PMC):
-
Transcatheter Aortic Valve Implantation and Conduction Disturbances: Focus on Clinical Implications.
Halapas A, Koliastasis L, Doundoulakis I, Antoniou CK, et al · · 2023 · cited 9× · PMID 37998527 · DOI 10.3390/jcdd10110469 -
Management of conduction disturbances after TAVI: the last step towards early discharge.
Muntané-Carol G, Romaguera R, Gómez-Hospital JA, Nuche J, et al · · 2025 · PMID 40607130 · DOI 10.26599/1671-5411.2025.05.004
Verify or expand the search:
- PubMed search for NCT05721170
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other recruiting trials for Aortic Valve Stenosis
Currently open trials in the same condition.
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Other National and Kapodistrian University of Athens trials
Trials by the same sponsor.
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- NCT07477496 — Recurrence and Anal Fistula Patient Reported Outcomes Trial · recruiting
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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 NCT05721170 (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 National and Kapodistrian University of Athens
- Last refreshed: 9 December 2024
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/NCT05721170.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing