Actively Recruiting

Age: 18Years +
All Genders
NCT07335627

Clindamycin as Antimicrobial Treatment for Streptococcus Spp. PeRiprosthetic Infection

Led by University Hospital, Strasbourg, France · Updated on 2026-01-13

260

Participants Needed

1

Research Sites

73 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Clindamycin is an antibiotic with several advantages: high oral bioavailability and good bone and joint penetration. In France, it is a recommended drug for other types of Streptococcus spp. osteoarticular infections and can be used as an alternative to amoxicillin for periprosthetic infections, including when implants are retained. The hypothesis of this study is that clindamycin is no less effective than other drugs commonly used to treat periprosthetic Streptococcus spp. infections. The primary objective of this study is to evaluate the success rate of Streptococcus spp. periprosthetic joint infections treated with clindamycin compared to other antibiotic treatments.

CONDITIONS

Official Title

Clindamycin as Antimicrobial Treatment for Streptococcus Spp. PeRiprosthetic Infection

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patient (aged 18 years or older) at the time of surgery for infection
  • Probable or proven periprosthetic infection with Streptococcus spp. according to EBJIS diagnostic criteria
  • Patient operated on in one of the associated centers between 2013 and 2024
Not Eligible

You will not qualify if you...

  • Patient who underwent joint resection or amputation
  • Patient who was treated with suppressive antibiotic therapy lasting more than 6 months decided upon prior to surgery

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Service de Chirurgie Orthopédique Septique - CHU de Strasbourg - France

Strasbourg, France, 67091

Actively Recruiting

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Research Team

S

Stéphane KLEIN, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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