Optilene® Suture for Coronary Artery Bypass Graft Surgery

NCT02546557 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 245

Last updated 2019-01-23

No results posted yet for this study

Summary

The study is a voluntary study, initiated by B. Braun to collect clinical data for Optilene® suture concerning its key indication.

Conditions

Interventions

PROCEDURE

Coronary Artery Bypass Graft surgery

Sponsors & Collaborators

  • B.Braun Surgical SA

    collaborator INDUSTRY
  • Aesculap AG

    lead INDUSTRY

Principal Investigators

  • Joseph M Padró, Prof. Dr. · Hospitla de la Santa Creu I Sant Pau

Eligibility

Min Age
25 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-11-10
Primary Completion
2018-10-31
Completion
2018-10-31

Countries

  • Germany
  • Italy
  • Portugal
  • Spain

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 NCT02546557 on ClinicalTrials.gov