Osteoarticular Infections With Pneumococcal
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
| ClinicalTrials.gov Identifier: NCT03852784 |
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Recruitment Status :
Completed
First Posted : February 25, 2019
Last Update Posted : January 19, 2022
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| Condition or disease | Intervention/treatment |
|---|---|
| Bone and Joint Infection | Other: Bone and joint infection with Streptococcus peumoniae |
| Study Type : | Observational |
| Actual Enrollment : | 33 participants |
| Observational Model: | Cohort |
| Time Perspective: | Retrospective |
| Official Title: | Osteoarticular Infections With Pneumococcal |
| Actual Study Start Date : | January 1, 2019 |
| Actual Primary Completion Date : | March 1, 2019 |
| Actual Study Completion Date : | April 1, 2020 |
| Group/Cohort | Intervention/treatment |
|---|---|
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Bone and joint infection with Streptococcus peumoniae
Patients having had an osteoarticular infection with Streptococcus peumoniae
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Other: Bone and joint infection with Streptococcus peumoniae
description of the osteoarticular infection with Streptococcus peumoniae |
- Description and rate of bone or joint infection with S. pneumoniae [ Time Frame: Outcome is measured at the end of follow-up (usually between 12 and 24 months after antibiotic therapy disruption ]Description of the type of infection due to S. pneumoniae : patients and type of implant, profile of the bacterium associated in the infection, medical and chirurgical treatment
- Rate of Treatment Failure [ Time Frame: Outcome is measured at the end of follow-up (usually between 12 and 24 months after antibiotic therapy disruption ]Treatment failure is defined by local clinical and/or microbiological relapse; and/or need for additional surgery; death of septic origin
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| Ages Eligible for Study: | 18 Years to 100 Years (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Sampling Method: | Non-Probability Sample |
Inclusion Criteria:
- patients having had a bone and joint infection with S pneumoniae, with or without device.
Exclusion Criteria:
- none
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03852784
| France | |
| Hospices Civils de Lyon | |
| Lyon, France, 69004 | |
| Study Director: | Tristan Ferry, Md,PhD | Hospices Civils de Lyon |
| Responsible Party: | Eugénie MABRUT, clinical reserach assistant, Hospices Civils de Lyon |
| ClinicalTrials.gov Identifier: | NCT03852784 |
| Other Study ID Numbers: |
19-074 |
| First Posted: | February 25, 2019 Key Record Dates |
| Last Update Posted: | January 19, 2022 |
| Last Verified: | April 2020 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | Undecided |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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Bone and Joint Infection Streptococcus peumoniae |
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Infections Communicable Diseases Disease Attributes Pathologic Processes |

