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Comparison of 30 days all-cause death of patients who are treated with balloon procedure (PETROS) vs. clot-dissolving medicines in patients with stuck mechanical heart valves

STUCK VALVE REGISTRY TRIAL - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/05/067331
Enrollment
1204
Registered
2024-05-14
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Health Condition 1: I083- Combined rheumatic disorders of mitral, aortic and tricuspid valves Health Condition 2: I351- Nonrheumatic aortic (valve) insufficiency Health Condition 3: I350- Nonrheumatic aortic (valve) stenosis Health Condition 4: I340- Nonrheumatic mitral (valve) insufficiency Health Condition 5: I341- Nonrheumatic mitral (valve) prolapse Health Condition 6: I998- Other disorder of circulatory system

Interventions

None listed

Sponsors

The Madras Medical Mission
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: The patients who underwent repeat surgery, fibrinolysis or PETROS for stuck valve from First January 2019 till the CTRI registration of this registry will be included retrospectively. From the completion of CTRI registration the participants will be included prospectively till 2029.

Exclusion criteria

Exclusion criteria: Not willing to participate.

Design outcomes

Primary

MeasureTime frame
All-cause mortalityTimepoint: 30days—

Secondary

MeasureTime frame
All-cause mortalityTimepoint: one-year—

Countries

India

Contacts

Public ContactDr Nandhakumar Vasu

The Madras Medical Mission

nandha.intervention@gmail.com9952516668

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026