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Antibiotic Treatment to Patients With Low Back Pain

Primary Purpose

Back Pain

Status
Completed
Phase
Phase 4
Locations
Denmark
Study Type
Interventional
Intervention
Bioclavid
Placebo
Sponsored by
The Back Research Center, Denmark
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Back Pain focused on measuring Low Back Pain,

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Age between 18-65 years Previous lumbar herniated disc confirmed by MRI Time since lumbar disc herniation more than 6 months less than 2 years LBP in the area of L1 to L5, with an added Low Back Pain Rating Scale of 6 or more The present MRI shows Modic changes Positive Springing test (SPT) at the level of Modic changes Exclusion Criteria: Allergy against antibiotics The Beck Depression Inventory >7, Pregnancy Breast feeding All Kidney diseases Pending workers litigation or pension Danish as second language Fertile women who do not user safe anti conseption Reduced liver functions Reduced liver function due to previous treatment wiht amoxicillin/clavulanasid.

Sites / Locations

  • The Back Research Center

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Placebo Comparator

Experimental

Placebo Comparator

Arm Label

Group A, Antibiotic

Group B: 1 placebo

Group C: Antibiotics

Group D, Placebo

Arm Description

1 antibiotic tablet 45 patients Group

1 placebo tablet

2 antibiotic tablets 45 patients

2 placebo tablets 36 patients

Outcomes

Primary Outcome Measures

Low Back Pain Roland Morris Questionaire

Secondary Outcome Measures

Full Information

First Posted
March 14, 2006
Last Updated
May 26, 2010
Sponsor
The Back Research Center, Denmark
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1. Study Identification

Unique Protocol Identification Number
NCT00302796
Brief Title
Antibiotic Treatment to Patients With Low Back Pain
Official Title
Antibiotic Treatment to Patients With Low Back Pain Associated With Modic Changes Following Disc Herniation. A Randomized Clinical Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
July 2009
Overall Recruitment Status
Completed
Study Start Date
March 2006 (undefined)
Primary Completion Date
October 2009 (Actual)
Study Completion Date
October 2009 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
The Back Research Center, Denmark

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
A large proportion of patients with Low Back Pain (LBP) (80 %) are classified as "non-specific", due to the lack of a patho-anatomical diagnosis. This term is not satisfactory, since it implies uncertainty for both the patient and the clinician. Modic changes have recently been identified as a pain giving patho-anatomical diagnosis for a considerable percentage (20-30 %) of LBP patients. The causes of these Modic changes have not been determined conclusively but bacterial infection is among the plausible causes for those following a disc herniation. Purpose The aim of this study is to assess the clinical effect of antibiotic treatment compared to placebo, in patients with LBP and Modic changes following a lumbar herniated disc. Design A double blind prospective clinically controlled trial. Patients will be randomized by a blinded observer to either Group A: 1 antibiotic tablet 45 patients Group B: 1 placebo tablet 36 patients Group C: 2 antibiotic tablets 45 patients Group D: 2 placebo tablets 36 patients The patients will take the drug three times a day for 100 days.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Back Pain
Keywords
Low Back Pain,

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
162 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Group A, Antibiotic
Arm Type
Experimental
Arm Description
1 antibiotic tablet 45 patients Group
Arm Title
Group B: 1 placebo
Arm Type
Placebo Comparator
Arm Description
1 placebo tablet
Arm Title
Group C: Antibiotics
Arm Type
Experimental
Arm Description
2 antibiotic tablets 45 patients
Arm Title
Group D, Placebo
Arm Type
Placebo Comparator
Arm Description
2 placebo tablets 36 patients
Intervention Type
Drug
Intervention Name(s)
Bioclavid
Intervention Description
500 + 125 mg times 3 or 6
Intervention Type
Drug
Intervention Name(s)
Placebo
Primary Outcome Measure Information:
Title
Low Back Pain Roland Morris Questionaire
Time Frame
One year follow-up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age between 18-65 years Previous lumbar herniated disc confirmed by MRI Time since lumbar disc herniation more than 6 months less than 2 years LBP in the area of L1 to L5, with an added Low Back Pain Rating Scale of 6 or more The present MRI shows Modic changes Positive Springing test (SPT) at the level of Modic changes Exclusion Criteria: Allergy against antibiotics The Beck Depression Inventory >7, Pregnancy Breast feeding All Kidney diseases Pending workers litigation or pension Danish as second language Fertile women who do not user safe anti conseption Reduced liver functions Reduced liver function due to previous treatment wiht amoxicillin/clavulanasid.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hanne B Albert, Ph.D
Organizational Affiliation
The Back Research Center, University of Southern Denmark
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Back Research Center
City
Ringe
ZIP/Postal Code
5230
Country
Denmark

12. IPD Sharing Statement

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Antibiotic Treatment to Patients With Low Back Pain

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