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Prospective, Single-arm, Multicenter Study for Evaluation the Safety and Effectiveness of the ALEX Stent in a Real-world Setting of Percutaneous Coronary Interventions in Patients With Coronary Heart Disease

NCT01637012 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2014-03-13

No results posted yet for this study

Summary

To evaluate the safety and effectiveness of the ALEX stent in a real-world setting of percutaneous coronary interventions in patients with coronary heart disease.

Conditions

Interventions

PROCEDURE

Implantation

index angioplasty with ALEX stent implatation

Sponsors & Collaborators

  • KCRI

    collaborator OTHER

  • Balton Sp.zo.o.

    lead INDUSTRY

Principal Investigators

  • Jacek Legutko, MD, PhD · Szpital Uniwersytecki w Krakowie, ul. Kopernika 17, Krakow 31-501, Poland

  • Dariusz Dudek, Prof. · Szpital Uniwersytecki w Krakowie, ul. Kopernika 17, Krakow 31-501, Poland

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-02-29
Primary Completion
2013-09-30
Completion
2013-09-30

Countries

  • Poland

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01637012 on ClinicalTrials.gov