Comparison of Two Antimicrobial Therapy Duration for Spondylodiscitis (DTS)
Primary Purpose
Vertebral Osteomyelitis
Status
Completed
Phase
Phase 4
Locations
France
Study Type
Interventional
Intervention
antibiotic
Sponsored by
About this trial
This is an interventional treatment trial for Vertebral Osteomyelitis focused on measuring Spondylodiscitis, Duration treatment, Antibiotic, men or women more than 18 years, proved bacterial spondylodiscitis, patient for which is decided a treatment antibiotic, the diagnosis on clinical, Radiological, microbiological criteria
Eligibility Criteria
Inclusion Criteria:
- men or women more than 18 years
- proved bacterial spondylodiscitis due to pyogenic germ (no mycobacteria, no fungus or brucella), for which is decided a treatment antibiotic
- diagnosis is based on clinical,radiological and microbiological criteria
- women in age to procreate, use of an effective contraception with protected sexual relations and negative pregnancy test (b HCG).
Exclusion Criteria:
- infection with no bacteriological identification
- infection due to mycobacteria, brucella or fungus
- presence of material
- recurrence of spondylodiscitis
- Patient whose life expectation is 1-year-old subordinate
- pregnant or breast-feeding Woman
Sites / Locations
- Chu Raymond Poincare
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
1
2
Arm Description
- group A : during 6 weeks after the inclusion
-group B : during 12 weeks after the inclusion
Outcomes
Primary Outcome Measures
Percentage of success in 1 year defined by the absence of infection : absence of clinical, biological and radiological signs of infection (pain, fever) ; or relapse with the same germ.
Secondary Outcome Measures
1)Effective antibiotherapy duration
2) Failure rate at 6 month
3)Rachidial pains (clinical examination and analogical visual scale of the pain) at every visit
4)Quality of life by the score EQ-5D at 6 and 12 month
5)Observance of the treatment measured at every visit
6)Appearance of microbial resistances estimated by comparison of antibiogram in case of failure
7)Antimicrobial therapy tolerance measure at each visit
8)Identification of risk factors for failure
Full Information
NCT ID
NCT00764114
First Posted
September 30, 2008
Last Updated
May 3, 2013
Sponsor
Assistance Publique - Hôpitaux de Paris
1. Study Identification
Unique Protocol Identification Number
NCT00764114
Brief Title
Comparison of Two Antimicrobial Therapy Duration for Spondylodiscitis
Acronym
DTS
Official Title
Comparison of Two Antimicrobial Therapy Duration (6 Weeks Versus 12 Weeks)for Spondylodiscitis
Study Type
Interventional
2. Study Status
Record Verification Date
February 2011
Overall Recruitment Status
Completed
Study Start Date
November 2006 (undefined)
Primary Completion Date
August 2012 (Actual)
Study Completion Date
April 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Duration of antimicrobial therapy for spondylodiscitis is not standardized; it could vary from 6 weeks to several months depending on the medical habits. The study hypothesis is that a 6 weeks antimicrobial therapy is not inferior to a 12 weeks.
We run a prospective multi-centric, non inferiority open label trial, randomised in two parallel groups.
The main objective is to compare the efficacy of two durations of antibiotherapy, 6 weeks versus 12 weeks, on the rate of cure in this indication.
The study concerns 400 patients more than 18 years, 70 centres in France are involved.
The duration of the study is 4 years.
Detailed Description
In France, incidence of spondylodiscitis is between 1000 and 1500 new cases a year. Micro-organisms mainly in cause are: Staphylococcus aureus, negative coagulase Staphylococcus, Gram negative bacilli and Streptococci; more rarely mycobacteria or Brucella. Actually, optimal duration of antimicrobial therapy is unclear. The rate of cure varies, according to studies, from 90 to 100 % whatever the responsible germ involved. If a 6 weeks antimicrobial therapy duration is not inferior to 12, this would allow to shortening usual antimicrobial therapy duration, and improve tolerance of the treatment, with ecological and economic benefits, following a politics of good use of antibiotics, defined in the French circular n°2002-272 of 02/05/02.
The main objective is to compare two durations of antimicrobial therapy, 6 weeks versus 12 weeks, on the rate of cure of the bacterial spondylodiscitis. Secondary objectives are to compare, according to the duration of treatment antibiotic, 1) Rachidial pain by clinical examination and an analogical visual scale (EVA), 2) Quality of life by the score EQ-5D, 3) Treatment tolerance. 4) Risk factors for failure.
Type of the study is Prospective multi-centric, open label trial, randomised in two parallel groups with direct individual profit.
Antimicrobial therapy is chosen by the physician on charge of the patient according to the germ and to the consensual recommendations.
The study concerns 400 patients.
Inclusion criteria are : men or women more than 18 years, having a proved bacterial spondylodiscitis (not mycobacteria, not fungal nor Brucella), for which an antimicrobial therapy is needed; for the women in age to procreate use of an effective contraception with protected sexual relations and negative pregnancy test (b HCG) is necessary.
Non Inclusion criteria are: infection with no bacteriological identification or mycobacteria, fungal or brucellosis infection, presence of material or recurrence of spondylodiscitis.
Main criterion of evaluation: percentage of success in 1 year defined by the absence of infection : absence of clinical, biological and radiological signs of infection (pain, fever) ; or relapse with the same germ.
This criterion will be estimated beyond the first 6 weeks of treatment antibiotic after the introduction of the treatment and until 1 year after the stop of the treatment. The criteria of the bacteriological diagnosis will be the same.
Design of the study: patients after information consent signed are include and randomised in one arm. They are regularly follow (at 1, 2, 3, 6 and 12 weeks after the beginning of antimicrobial therapy, then at 6 and 12 month after the end of antimicrobial therapy) , with physical examination, biological tests and radiological acts.
The randomisation is centralized, balanced by block, stratifies by centres. (70 centres) The previous duration of the study is of 4 years.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vertebral Osteomyelitis
Keywords
Spondylodiscitis, Duration treatment, Antibiotic, men or women more than 18 years, proved bacterial spondylodiscitis, patient for which is decided a treatment antibiotic, the diagnosis on clinical, Radiological, microbiological criteria
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
351 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Active Comparator
Arm Description
- group A : during 6 weeks after the inclusion
Arm Title
2
Arm Type
Active Comparator
Arm Description
-group B : during 12 weeks after the inclusion
Intervention Type
Drug
Intervention Name(s)
antibiotic
Intervention Description
6 or 12 weeks
Primary Outcome Measure Information:
Title
Percentage of success in 1 year defined by the absence of infection : absence of clinical, biological and radiological signs of infection (pain, fever) ; or relapse with the same germ.
Time Frame
1 year after the stop of the treatment.
Secondary Outcome Measure Information:
Title
1)Effective antibiotherapy duration
Time Frame
12 months
Title
2) Failure rate at 6 month
Time Frame
6 months
Title
3)Rachidial pains (clinical examination and analogical visual scale of the pain) at every visit
Time Frame
6 an 12 month
Title
4)Quality of life by the score EQ-5D at 6 and 12 month
Time Frame
6 and 12 month
Title
5)Observance of the treatment measured at every visit
Time Frame
6 and 12 month
Title
6)Appearance of microbial resistances estimated by comparison of antibiogram in case of failure
Time Frame
during 12 months
Title
7)Antimicrobial therapy tolerance measure at each visit
Time Frame
6 and 12 month
Title
8)Identification of risk factors for failure
Time Frame
during 12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
men or women more than 18 years
proved bacterial spondylodiscitis due to pyogenic germ (no mycobacteria, no fungus or brucella), for which is decided a treatment antibiotic
diagnosis is based on clinical,radiological and microbiological criteria
women in age to procreate, use of an effective contraception with protected sexual relations and negative pregnancy test (b HCG).
Exclusion Criteria:
infection with no bacteriological identification
infection due to mycobacteria, brucella or fungus
presence of material
recurrence of spondylodiscitis
Patient whose life expectation is 1-year-old subordinate
pregnant or breast-feeding Woman
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Louis Bernard, PU-PH
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Principal Investigator
Facility Information:
Facility Name
Chu Raymond Poincare
City
Garches
ZIP/Postal Code
92380
Country
France
12. IPD Sharing Statement
Citations:
PubMed Identifier
26438497
Citation
Desoutter S, Cottier JP, Ghout I, Issartel B, Dinh A, Martin A, Carlier R, Bernard L; Duration of Treatment for Spondylodiscitis Study Group. Susceptibility Pattern of Microorganisms Isolated by Percutaneous Needle Biopsy in Nonbacteremic Pyogenic Vertebral Osteomyelitis. Antimicrob Agents Chemother. 2015 Dec;59(12):7700-6. doi: 10.1128/AAC.01516-15. Epub 2015 Oct 5.
Results Reference
derived
PubMed Identifier
25984880
Citation
Zervou FN, Zacharioudakis IM, Mylonakis E. ACP Journal Club. 6 weeks of antibiotics was noninferior to 12 weeks for clinical cure in pyogenic vertebral osteomyelitis. Ann Intern Med. 2015 May 19;162(10):JC7. doi: 10.7326/ACPJC-2015-162-10-007. No abstract available.
Results Reference
derived
PubMed Identifier
25468170
Citation
Bernard L, Dinh A, Ghout I, Simo D, Zeller V, Issartel B, Le Moing V, Belmatoug N, Lesprit P, Bru JP, Therby A, Bouhour D, Denes E, Debard A, Chirouze C, Fevre K, Dupon M, Aegerter P, Mulleman D; Duration of Treatment for Spondylodiscitis (DTS) study group. Antibiotic treatment for 6 weeks versus 12 weeks in patients with pyogenic vertebral osteomyelitis: an open-label, non-inferiority, randomised, controlled trial. Lancet. 2015 Mar 7;385(9971):875-82. doi: 10.1016/S0140-6736(14)61233-2. Epub 2014 Nov 5.
Results Reference
derived
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Comparison of Two Antimicrobial Therapy Duration for Spondylodiscitis
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