The Direct III Post Market Study

NCT02693158 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 440

Last updated 2020-06-26

No results posted yet for this study

Summary

The primary objective of this multicenter, single-arm, observational study is to evaluate the feasibility of a systematic direct stenting strategy with the Svelte SLENDER IDS Sirolimus-Eluting Coronary Stent-on-a-Wire Integrated Delivery System (SLENDER IDS) in an all-comers, real-world population.

Conditions

Sponsors & Collaborators

  • Svelte Medical Systems, Inc.

    lead INDUSTRY

Principal Investigators

  • Dennis Donohoe, MD · Svelte Medical

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-09-30
Primary Completion
2019-01-31
Completion
2020-01-31

Countries

  • Netherlands

Study Locations

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Entities

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 NCT02693158 on ClinicalTrials.gov