Treatment of Methicillin-sensitive Staphylococcus Aureus (MSSA) (CLINDOS)

The recruitment status of this study is unknown because the information has not been verified recently.
Verified September 2010 by Assistance Publique - Hôpitaux de Paris.
Recruitment status was  Active, not recruiting
Sponsor:
Information provided by (Responsible Party):
Assistance Publique - Hôpitaux de Paris
ClinicalTrials.gov Identifier:
NCT01500837
First received: November 28, 2011
Last updated: January 3, 2012
Last verified: September 2010

November 28, 2011
January 3, 2012
October 2010
December 2012   (final data collection date for primary outcome measure)
Measurement of peak and trough serum concentrations of clindamycin [ Time Frame: 1 month ] [ Designated as safety issue: No ]
Measurement of peak and trough serum concentrations of clindamycin will be performed at Day 1, Day 15 and Day 30
Same as current
Complete list of historical versions of study NCT01500837 on ClinicalTrials.gov Archive Site
proportion of patients healing (as determined from absence of fever, absence of pain and favorable aspect of scar). [ Time Frame: Day 30 ] [ Designated as safety issue: No ]
Same as current
Not Provided
Not Provided
 
Treatment of Methicillin-sensitive Staphylococcus Aureus (MSSA)
Treatment of Methicillin-sensitive Staphylococcus Aureus Orthopaedic Infections With Clindamycin in Combination With Rifampin or Levofloxacin: a Randomized Pharmacological and Clinical Study (the CLINDOS Trial)

Background:

One of the leading causes of peri-operative osteoarticular infections (OAI) is Staphylococcus aureus. Treatment usually requires surgical debridement in association with appropriate antibiotic therapy. After surgery, an intravenous (IV) antibiotic therapy is routinely indicated for 10 to 15 days, followed by a minimal one-month oral treatment. In this protocol, the latter includes clindamycin in combination with rifampin or levofloxacin. Clindamycin is considered a good option in staphylococcal infections, because of its action against biofilm formation and bacterial adherence, its high level of joint and bone penetration and its good tolerance. Rifampin, a potent cytochrome P-450 inducer, enhances the elimination of a large number of drugs. Therefore, an influence of rifampin on clindamycin pharmacokinetics must be considered.

Objectives:

The primary objective is to compare the influence of rifampin and levofloxacin respectively on the pharmacokinetics of clindamycin in a randomized series of peri-operative staphylococcal OAI. The investigators then seek to determine the optimal drug association with regard to infection control and drug tolerance.

Study design:

Monocentric, randomized, open label, comparative study

Study period:

From November 2010 to October 2011.

Materials and Methods:

Following surgical debridement and after 10 to 15 days of IV antibiotherapy, patients are randomly assigned either to the "clindamycin/rifampin" arm either to the "clindamycin/levofloxacin" arm, according to the antimicrobial susceptibility testing. Peak and trough serum concentrations of clindamycin are measured at day-1, day-15 and day-30 of oral treatment. Rifampin and levofloxacin serum concentrations are measured at the same intervals to monitor patient compliance.

Background:

One of the leading causes of peri-operative osteoarticular infections (OAI) is Staphylococcus aureus. Treatment usually requires surgical debridement in association with appropriate antibiotic therapy. After surgery, an intravenous (IV) antibiotic therapy is routinely indicated for 10 to 15 days, followed by a minimal one-month oral treatment. In this protocol, the latter includes clindamycin in combination with rifampin or levofloxacin. Clindamycin is considered a good option in staphylococcal infections, because of its action against biofilm formation and bacterial adherence, its high level of joint and bone penetration and its good tolerance. Rifampin, a potent cytochrome P-450 inducer, enhances the elimination of a large number of drugs. Therefore, an influence of rifampin on clindamycin pharmacokinetics must be considered.

Objectives:

The primary objective is to compare the influence of rifampin and levofloxacin respectively on the pharmacokinetics of clindamycin in a randomized series of peri-operative staphylococcal OAI. The investigators then seek to determine the optimal drug association with regard to infection control and drug tolerance. Study design: monocentric, randomized, open label, comparative study

Study period:

From November 2010 to October 2011.

Materials and Methods:

Following surgical debridement and after 10 to 15 days of IV antibiotherapy, patients are randomly assigned either to the "clindamycin/rifampin" arm either to the "clindamycin/levofloxacin" arm, according to the antimicrobial susceptibility testing. Peak and trough serum concentrations of clindamycin are measured at day-1, day-15 and day-30 of oral treatment. Rifampin and levofloxacin serum concentrations are measured at the same intervals to monitor patient compliance. Infection cure is evaluated clinically, with periodic X-rays and CRP dosage in serum.

Interventional
Not Provided
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Osteoarticular Infection
  • Drug: association of RIFAMPIN + CLINDAMYCIN
    association of RIFAMPIN + CLINDAMYCIN
    Other Name: RIFAMPIN
  • Drug: association of LEVOFLOXACIN+ CLINDAMYCIN
    association of LEVOFLOXACIN+ CLINDAMYCIN
    Other Name: LEVOFLOXACIN
  • Active Comparator: RIFAMPIN
    CLINDAMYCIN + RIFAMPIN
    Intervention: Drug: association of RIFAMPIN + CLINDAMYCIN
  • Active Comparator: LEVOFLOXACIN
    CLINDAMYCIN + LEVOFLOXACIN
    Intervention: Drug: association of LEVOFLOXACIN+ CLINDAMYCIN
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Active, not recruiting
23
December 2012
December 2012   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • subject over 18 years with a IOA with GERME sensitivity to three antibiotics,
  • Patient in orthopedic unit of HEGP,
  • Patient who received and understood the information and who signed consent,

Exclusion Criteria:

  • Known allergy to one of three antibiotics and / or excipients,
  • Pregnancy or during lactation,
  • Congenital galactosemia, malabsorption of glucose and galactose, or lactase deficiency,
  • History of tendinopathy with fluoroquinolones,
  • G6PD deficiency,
  • porphyria,
  • subject receiving a protease inhibitor,
  • subject receiving anticoagulants
  • Malabsorption syndrome,
  • subject unable to follow the protocol (organizational problem, intellectual disability, ...).
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
France
 
NCT01500837
K000000
No
Assistance Publique - Hôpitaux de Paris
Assistance Publique - Hôpitaux de Paris
Not Provided
Study Director: Brigitte Sabatier, PD, PhD Department of Pharmacology
Assistance Publique - Hôpitaux de Paris
September 2010

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP