Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Clindamycin and rifampicin are authorized in osteoarticular infection treatment (IDSA guidelines) but some interaction is observed. The objective of this study is to evaluate and quantify rifampicin interaction on clindamycin
It could suggest modification of recommended doses or incitement to antibiotic dosage. Thus, theses antibiotics, if association is allowed, could limit fluoroquinolones prescription and avoid some antibiotic resistance.
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Clindamycin and rifampicin dosages | Other | blood samples for clindamycin and rifampicin dosages (for each patient) |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Clindamycin and rifampicin dosages | Biological | blood samples for clindamycin and rifampicin dosages (for each patient) |
|
| Measure | Description | Time Frame |
|---|---|---|
| clindamycin AUC (area under curve) at steady state and after rifampicin introduction | this AUC of clindamycin will be compared to AUC before rifampicin introduction, at day 0 | clindamycin AUC will be evaluated after rifampicin interaction, so at day 14 of introduction |
| Measure | Description | Time Frame |
|---|---|---|
| rifampicin auto induction | rifampicin autoinduction will be studied with rifampicin AUC, according time, for each patient, at day 4 and day 14. Comparison of AUC with student's test | AUC of rifampicin at day 4 (before autoinduction ant at steady state) and day 14 (after autoinduction) |
| clinical outcome |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Tiphaine Goulenok, MD | Assistance Publique - Hôpitaux de Paris | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Service de Médecine Interne - Hôpital Bichat Claude Bernard | Paris | 75018 | France |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| ID | Term |
|---|---|
| D013203 | Staphylococcal Infections |
| ID | Term |
|---|---|
| D016908 | Gram-Positive Bacterial Infections |
| D001424 | Bacterial Infections |
| D001423 | Bacterial Infections and Mycoses |
| D007239 | Infections |
Not provided
Not provided
| ID | Term |
|---|---|
| D002981 | Clindamycin |
| ID | Term |
|---|---|
| D008034 | Lincomycin |
| D055231 | Lincosamides |
| D011759 | Pyrrolidines |
| D006573 | Heterocyclic Compounds, 1-Ring |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
resolution of symptoms first described (pain, swelling, fever…) with specific scale |
| at day 4, day 14, day 28 (or day 60 if osteosynthesis) |
| biological outcome | resolution of inflammatory syndrome (measure of C reactive protein) and hyperleucocytosis (WBC) | at day 4, day 14, day 28 (or day 60 if osteosynthesis) |
| side effects and toxicity: number of participants with treatment related adverse events as assessed by CTCAE v4.0 | skin lesion, digestive symptoms, clostridium infection, liver cytolysis, hematological disorders (leucopenia, hemolytic anemia, thrombopenia)… | at day 2, day 4, day 14, day 28 (or day 60 if osteosynthesis) |
| D006571 |
| Heterocyclic Compounds |
| D006027 | Glycosides |
| D002241 | Carbohydrates |