Rifampin Combination Therapy Versus Monotherapy in Early Staphylococcal Infections After Total Hip and Knee Arthroplasty
Primary Purpose
Prosthesis-related Infections, Staphylococcal Infections
Status
Unknown status
Phase
Phase 4
Locations
Norway
Study Type
Interventional
Intervention
Rifampin-combination therapy
Monotherapy
Sponsored by
About this trial
This is an interventional treatment trial for Prosthesis-related Infections
Eligibility Criteria
Inclusion Criteria:
- Prosthetic joint infections category 2 or 3 (early post.op infections within 4 weeks).
- Diagnosis of staphylococci.
- Clinically and radiographically stable implants kept in place after revision.
Exclusion Criteria:
- Infection with other microorganisms than staphylococci.
- Less than 2 years of expected survival.
- Predictable inability to comply with the treatment and/or follow-up visits.
- Contraindication to the use of study medication including acute or chronic liver disease.
- Lack of written consent.
- Fertile women.
- Patients taking less than 80% of the study medication.
Sites / Locations
- Buskerud Central Hospital
- Elverum Hospital
- Martina Hansen Hospital
- Ringerike Hospital
- Lillehammer Hospital
- Oslo University Hospital, Ulleval
- Asker and Bærum Hospital
- St.Olav Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Rifampicin-combination therapy
Monotherapy
Arm Description
Cloxacillin or vancomycin in combination with Rifampicin. Treatment of early staphylococcal prosthetic joint infections in addition to debridement and retention of the prosthesis.
Cloxacillin or vancomycin in the treatment of early staphylococcal prosthetic joint infections in addition to debridement and retention of the prosthesis.
Outcomes
Primary Outcome Measures
Cure defined as lack of clinical, biochemistry or radiological signs of infection at two years follow-up.
Secondary Outcome Measures
Full Information
NCT ID
NCT00423982
First Posted
January 17, 2007
Last Updated
June 26, 2013
Sponsor
Oslo University Hospital
1. Study Identification
Unique Protocol Identification Number
NCT00423982
Brief Title
Rifampin Combination Therapy Versus Monotherapy in Early Staphylococcal Infections After Total Hip and Knee Arthroplasty
Official Title
Rifampin Combination Therapy Versus Monotherapy in Early Staphylococcal Infections After Total Hip and Knee Arthroplasty
Study Type
Interventional
2. Study Status
Record Verification Date
June 2013
Overall Recruitment Status
Unknown status
Study Start Date
April 2006 (undefined)
Primary Completion Date
December 2012 (Actual)
Study Completion Date
December 2014 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Oslo University Hospital
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The number of patients requiring joint replacement is increasing due to its success in restoring function and pain relief, and the growing population of the elderly. One of the most serious complications of arthroplasty is joint prosthesis infection. Due to the absence of prospective, randomized, controlled studies, there is no consensus concerning diagnosis and treatment of prosthetic joint infections. The main objective of this trial is to evaluate the clinical efficacy of rifampin combination therapy versus monotherapy using cloxacillin or vancomycin in early staphylococcal infections after total hip and knee arthroplasty.
Detailed Description
The study is a controlled randomized multicentre trial with 8 participating centres in Norway. We will include patients with the diagnosis of early infections (within 4 weeks post operatively)after hip or knee replacement. Patients with clinical signs of infection are scheduled for a standardized soft tissue revision. Diagnosis of staphylococci must be established by arthrocentesis or at surgical revision, and must grow in at least 2/8 cultures.The patients will randomly be assigned to antimicrobial therapy with or without rifampin by a randomization programme. Antibiotics will be given for 6 weeks. Two years follow-up. The study end points are final follow-up visit after two years or relapse of infection.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prosthesis-related Infections, Staphylococcal Infections
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Rifampicin-combination therapy
Arm Type
Active Comparator
Arm Description
Cloxacillin or vancomycin in combination with Rifampicin. Treatment of early staphylococcal prosthetic joint infections in addition to debridement and retention of the prosthesis.
Arm Title
Monotherapy
Arm Type
Active Comparator
Arm Description
Cloxacillin or vancomycin in the treatment of early staphylococcal prosthetic joint infections in addition to debridement and retention of the prosthesis.
Intervention Type
Drug
Intervention Name(s)
Rifampin-combination therapy
Other Intervention Name(s)
Antimicrobial therapy in prosthetic joint infection., Rifampicin and prosthetic joint infection.
Intervention Description
Rifampin 300 mg x 3 po and cloxacillin 2 g x 4 iv for two weeks. Then rifampin 300 mg x 3 po and cloxacillin 1 g x 4 po for 4 weeks. In case of methicillin resistance, rifampin 300 mg x 3 po and vancomycin 1 g x 2 iv for 6 weeks.
Intervention Type
Drug
Intervention Name(s)
Monotherapy
Other Intervention Name(s)
Antimicrobial therapy in prosthetic joint infections., Cloxacillin., Vancomycin.
Intervention Description
Cloxacillin 2 g x 4 iv for two weeks, then cloxacillin 1 g x 4 po for 4 weeks. In case of methicillin resistance, vancomycin 1 g x 2 iv for 6 weeks.
Primary Outcome Measure Information:
Title
Cure defined as lack of clinical, biochemistry or radiological signs of infection at two years follow-up.
Time Frame
2 years
10. Eligibility
Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Prosthetic joint infections category 2 or 3 (early post.op infections within 4 weeks).
Diagnosis of staphylococci.
Clinically and radiographically stable implants kept in place after revision.
Exclusion Criteria:
Infection with other microorganisms than staphylococci.
Less than 2 years of expected survival.
Predictable inability to comply with the treatment and/or follow-up visits.
Contraindication to the use of study medication including acute or chronic liver disease.
Lack of written consent.
Fertile women.
Patients taking less than 80% of the study medication.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Finnur Snorrason, M.D, Ph.D
Organizational Affiliation
Ullevaal University Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Buskerud Central Hospital
City
Drammen
ZIP/Postal Code
3004
Country
Norway
Facility Name
Elverum Hospital
City
Elverum
ZIP/Postal Code
2408
Country
Norway
Facility Name
Martina Hansen Hospital
City
Gjettum
ZIP/Postal Code
1346
Country
Norway
Facility Name
Ringerike Hospital
City
Hønefoss
ZIP/Postal Code
3504
Country
Norway
Facility Name
Lillehammer Hospital
City
Lillehammer
ZIP/Postal Code
2609
Country
Norway
Facility Name
Oslo University Hospital, Ulleval
City
Oslo
ZIP/Postal Code
0407
Country
Norway
Facility Name
Asker and Bærum Hospital
City
Rud
ZIP/Postal Code
1309
Country
Norway
Facility Name
St.Olav Hospital
City
Trondheim
ZIP/Postal Code
7030
Country
Norway
12. IPD Sharing Statement
Citations:
PubMed Identifier
32859235
Citation
Karlsen OE, Borgen P, Bragnes B, Figved W, Grogaard B, Rydinge J, Sandberg L, Snorrason F, Wangen H, Witsoe E, Westberg M. Rifampin combination therapy in staphylococcal prosthetic joint infections: a randomized controlled trial. J Orthop Surg Res. 2020 Aug 28;15(1):365. doi: 10.1186/s13018-020-01877-2.
Results Reference
derived
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Rifampin Combination Therapy Versus Monotherapy in Early Staphylococcal Infections After Total Hip and Knee Arthroplasty
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