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Postoperative events and 1 year outcome of aortic valve surgery with Perceval plus valve

PERCEIVE-IN (Perceval PLUS Effectiveness and Real-world Clinical Evaluation In Vivo in Indian Population) - PERCEIVE-IN

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/03/082063
Enrollment
200
Registered
2025-03-10
Start date
Unknown
Completion date
Unknown
Last updated
2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: I39- Endocarditis and heart valve disorders in diseases classified elsewhere Health Condition 2: I359- Nonrheumatic aortic valve disorder, unspecified

Interventions

Intervention1: NIL: NA Control Intervention1: NIL: NA

Sponsors

Parekh Integrated Services Pvt Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Adult patients of either gender undergoing implantation with Perceval plus for aortic valve disease

Exclusion criteria

Exclusion criteria: 1.Patients not willing to participate in the study

Design outcomes

Primary

MeasureTime frame
Postoperative complications in patients with Perceval PLUS sutureless prosthetic aortic valve implantTimepoint: 30 Days—

Secondary

MeasureTime frame
1.Clinical and hemodynamic changes post Perceval PLUS implantation 2.All-cause mortality and morbidity 1 year post implantation of Perceval PLUSTimepoint: 30 Days and 1 year—

Countries

India

Contacts

Public ContactDrPradeep Narayan

Narayana Hrudayalaya Limited

pradeep.narayan.dr@narayanahealth.org8017249115

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Sep 19, 2026