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NCT03258333
Small Aortic Annulus - a New Solution to the Old Problem
trial testing aortic valve replacement in Aortic Valve Replacement in 60 participants. Status unknown.
1 January 2022
Quick facts
| Lead sponsor | The Federal Centre of Cardiovascular Surgery, Russia |
|---|---|
| Status | Status unknown |
| Study type | OBSERVATIONAL |
| Enrollment | 60 |
| Start date | 18 February 2017 |
| Primary completion | 1 January 2022 |
| Estimated completion | 1 July 2022 |
| Sites | 1 location across Russia |
Drugs / interventions tested
- aortic valve replacement
Conditions studied
- Aortic Valve Replacement — all drugs for Aortic Valve Replacement →
Sponsor
The Federal Centre of Cardiovascular Surgery, Russia
Who can join
Adults 60 to 90, any sex, with Aortic Valve Replacement. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
In this prospective single-center study included 60 patients with a severe degenerative aortic stenosis and small aortic annulus (\<21 mm) who underwent standard AVR with stented bioprosthesis (group 1, n=30) and aortic valve reconstruction using autologus pericardium (Ozaki procedure) (group 2, n=30)
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT03258333
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
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Related trials
Other trials of aortic valve replacement
Trials testing the same drug.
- NCT03667365 — Randomized Study for the Optimal Treatment of Symptomatic Patients With Low Gradient Severe Aortic Valve Stenosis and Pr · NA · terminated
- NCT03976817 — Aortic Valve Replacement Above the Aortic Annulus (SA-AVR) With the Carpentier-Edwards Magna-Ease Bioprosthesis · completed
Other recruiting trials for Aortic Valve Replacement
Currently open trials in the same condition.
- NCT07123480 — The Role of 4 Different Consent Approaches on a Pilot Study to Increase Cardiac Rehabilitation Attendance · NA · active not recruiting
- NCT05295628 — Evaluation of Safety and Effectiveness of the EMBLOK EPS During TAVR · NA · active not recruiting
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 NCT03258333 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by The Federal Centre of Cardiovascular Surgery, Russia
- Last refreshed: 23 August 2017
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/NCT03258333.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing