Bone and Joint Infection Clinical Trial
Official title:
Implant-Associated P. Aeruginosa Bone And Joint Infections : Experience In A Regional Reference Center In France
NCT number | NCT03624855 |
Other study ID # | 18-176 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | March 1, 2018 |
Est. completion date | May 1, 2018 |
Verified date | August 2018 |
Source | Hospices Civils de Lyon |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The aim of this study is to describe the bone or joint infection due to Pseudomonas aeruginosa in patients having implant.
Status | Completed |
Enrollment | 94 |
Est. completion date | May 1, 2018 |
Est. primary completion date | May 1, 2018 |
Accepts healthy volunteers | |
Gender | All |
Age group | 18 Years to 100 Years |
Eligibility |
Inclusion Criteria: - patients having BJI on implant caused by Pseudomonas aeruginosa Exclusion Criteria: |
Country | Name | City | State |
---|---|---|---|
France | Hospices Civils de Lyon | Lyon |
Lead Sponsor | Collaborator |
---|---|
Hospices Civils de Lyon |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Description and rate of bone or joint infection on implant caused due to Pseudomonas aeruginosa | Description of the type of infection due to P. aeruginosa : patients and type of implant, profile of the bacterium, medical and chirurgical treatment, rate | Outcome is measured at the end of follow-up (usually between 12 and 24 months after antibiotic therapy disruption) | |
Secondary | Rate of adverse events occurring under medical treatment against Pseudomonas aeruginosa | description of adverse events occurring under medical treatment against Pseudomonas aeruginosa in BJI | Outcome is measured at the end of follow-up (usually between 12 and 24 months after antibiotic therapy disruption) | |
Secondary | Rate of Treatment Failure | Treatment failure is defined by local clinical and/or microbiological relapse; and/or need for additional surgery; death of septic origin | Outcome is measured at the end of follow-up (usually between 12 and 24 months after antibiotic therapy disruption) |
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