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A Multi Center Study to Evaluate the Clinical Outcomes of Patients Undergoing Coronary Angioplasty with Evermine 50 Stent.

A Prospective, Multi Center Single Arm Study on Clinical Outcomes in Patients Undergoing PCI with Evermine 50 in a Large Population. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/02/104449
Enrollment
5000
Registered
2026-02-20
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Health Condition 1: I251- Atherosclerotic heart disease of native coronary artery

Interventions

Intervention1: Nil: Nil

Sponsors

Dr Mathew Iype
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Adults aged equal and above 18 years. 2. Patients undergoing PCI with implantation of the Evermine 50 stent. 3.Patient has given written informed consent for participation prior to enrolment. 4.Patient is willing to undergo all study procedures and follow-up requirements.

Exclusion criteria

Exclusion criteria: 1. Hypersensitivity or allergy to aspirin, heparin, clopidogrel ticlopidine drug such as Everolimus or similar drugs or any analogue or derivative cobalt chromium nickel molybdenum tungsten or any contrast media. 2. Patientin whom antiplatelet and or anticoagulant therapy are contraindicated. 3. Life expectancy of less than 1 year due to non-cardiac comorbidities. 4. Pregnant or lactating females. 5. Any condition that in the opinion of the Investigator would preclude safe participation in the study.

Design outcomes

Primary

MeasureTime frame
Target Lesion FailureTimepoint: 1 Year

Secondary

MeasureTime frame
Target Lesion Failure (TLF)Timepoint: 30 days 6 months;Cardiovascular deathTimepoint: 30 days, 6 months, 1 year;Target Vessel Myocardial InfarctionTimepoint: 30 days, 6 months, 1 year;Clinically-Driven TLR (CD-TLR)Timepoint: 30 days, 6 months, 1 year;Stent Thrombosis (ST) RateTimepoint: 30 days, 6 months, 1 year;Target Vessel Revascularization (TVR)Timepoint: 30 days, 6 months, 1 year;Target Vessel Failure (TVF)Timepoint: 30 days, 6 months, 1 year;Device successTimepoint: Index Procedure;Procedure successTimepoint: Discharge

Countries

India

Contacts

Public ContactMathew Iype

Medical College Hospital, Trivandrum

mathewiype2334@gmail.com9847188112

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026