Study to Check the safety and performance of Vector® PTCA Balloon Catheter

A retrospective, single-arm, multi-center, observational, post-market clinical follow-up study to evaluate the safety and performance of Vector® PTCA Balloon Catheter in real-world settings.

Status

Active, not recruiting

Phases

Phase 4

Study type

Observational

Source

CTRI

Registry ID

CTRI/2023/09/057758

Enrollment

125

Registered

2023-09-18

Start date

Unknown

Completion date

Unknown

Last updated

2023-10-16

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

Conditions

Health Condition 1: I21A- Other type of myocardial infarction

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Patients who had been treated with Vector PTCA balloon Catheter.

Exclusion criteria

Exclusion criteria: None

Design outcomes

Primary

Measure	Time frame
Major Adverse Cardiac EventsTimepoint: 12 Months	—

Secondary

Measure	Time frame
Procedural success Device Success Cardiac death Myocardial Infarction Target Vessel RevascularizationTimepoint: 12 Months	—

Countries

India

Contacts

Public ContactPreeti Vani

Maharaja Agrasen Hospital

drkumarabhishek39@gmail.com9800449121

Outcome results