Actively Recruiting

All Genders
NCT04724603

Phage Safety Retrospective Cohort Study

Led by Hospices Civils de Lyon · Updated on 2023-04-13

25

Participants Needed

1

Research Sites

291 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The aim of this study is to determine the imputability of adverse events in patients who have had phage therapy for the treatment of their bone or joint or implant infection, in order to find out whether these adverse effects are related to surgery, antibiotic treatment or bacteriophages.

CONDITIONS

Official Title

Phage Safety Retrospective Cohort Study

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients having had a bone, joint, or implant infection treated by phagotherapy
  • Patients who experienced an adverse event following phagotherapy treatment
Not Eligible

You will not qualify if you...

  • None specified

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
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3
+1

Trial Site Locations

Total: 1 location

1

Hospices Civils de Lyon

Lyon, France, 69004

Actively Recruiting

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How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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