A Randomized Study of Three Medication Regimens for Acute Low Back Pain
Primary Purpose
Acute Low Back Pain
Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Naproxen
Cyclobenzaprine
Oxycodone/ acetaminophen
Sponsored by

About this trial
This is an interventional treatment trial for Acute Low Back Pain focused on measuring low back pain
Eligibility Criteria
Inclusion Criteria:
- Non-radicular, non-traumatic low back pain of no more than 2 weeks duration
Exclusion Criteria:
- Back pain longer than 2 weeks
- Prior to the acute attack of low back pain, back pain once per month or more frequently
- Prior to the acute attack of low back pain, daily or near daily use of pain medication
Sites / Locations
- Montefiore Medical Center
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Active Comparator
Active Comparator
Arm Label
Opioid
Skeletal muscle relaxant
Naproxen alone
Arm Description
Naproxen + opioid
Naproxen + skeletal muscle relaxant
Naproxen + placebo
Outcomes
Primary Outcome Measures
Change in Functional Disability as Measured by the Roland Morris Disability Questionnaire
The Roland Morris Disability Questionnaire (RMDQ) is a 24 item instrument that evaluates the impact of low back pain on one's daily life. It is most sensitive for patients with mild to moderate disability due to acute, sub-acute or chronic low back pain. Each question can be answered as either a "yes" or "no". The score ranges from 0 to 24 where a higher score reflects greater impairment and, therefore, worsening in the quality of life. The change in RMDQ is obtained by subtracting the RMDQ score at one week after discharge from the baseline score.
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01587274
Brief Title
A Randomized Study of Three Medication Regimens for Acute Low Back Pain
Official Title
A Randomized Three-armed Comparative Effectiveness Study of Various Medications for Musculoskeletal Low Back Pain: Defining the Added Benefit of Muscle Relaxants and Opioids.
Study Type
Interventional
2. Study Status
Record Verification Date
July 2018
Overall Recruitment Status
Completed
Study Start Date
April 2012 (undefined)
Primary Completion Date
October 2014 (Actual)
Study Completion Date
December 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Montefiore Medical Center
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Low back pain causes 2.4% of visits to US emergency departments (ED) resulting in 2.7 million visits annually. In a general low back pain (LBP) population, prognosis is poor. About 50% of patients who visited general practitioners with new onset musculoskeletal LBP report persistent pain and functional disability three months after the index visit. Outcomes are similarly poor for the population of patients forced to use an ED for management of their LBP. In an observational study of patients with non-traumatic LBP recently completed at the PI's institution, patients were contacted one week after ED discharge: 70% reported persistent back-pain related functional impairment, 59% reported moderate or severe LBP, and 69% reported analgesic use within the previous 24 hours. Three months after the ED visit, 48% reported functional impairment, 42% reported moderate or severe pain, and 46% reported analgesic use within the previous 24 hours.
A variety of evidence-based medications are available to treat LBP. Non-steroidal anti-inflammatory drugs (NSAID) are more efficacious than placebo with regard to pain relief, global improvement, and requirement of analgesic medication. Skeletal muscle-relaxants too are effective for short-term pain relief and global efficacy. Opioids are commonly used for moderate or severe acute LBP,(9) though high-quality evidence supporting this practice is lacking.
Treatment of LBP with multiple concurrent medications is common in the ED setting. Emergency physicians often prescribe NSAIDs, skeletal muscle relaxants, and opioids in combination. Several clinical trials have compared combination therapy with NSAIDS+ skeletal muscle relaxants to monotherapy with just one of these agents. These trials have reported heterogeneous results. The combination of opioids + NSAIDS has not been evaluated experimentally in patients with acute LBP.
Given the poor pain and functional outcomes that persist beyond an ED visit for musculoskeletal LBP, the investigators propose a clinical trial to evaluate whether combining muscle relaxants or opioids with NSAIDs is more effective than NSAID monotherapy for the treatment of non-traumatic, non-radicular low back pain. Specifically, the investigators will evaluate three distinct hypotheses:
The combination of naproxen + cyclobenzaprine will provide greater relief of LBP than naproxen alone seven days after an ED visit, as measured by the Roland Morris low back pain functional disability scale
The combination of naproxen + oxycodone/ acetaminophen will provide greater relief of LBP than naproxen alone seven days after an ED visit, as measured by the Roland Morris low back pain functional disability scale
The combination of naproxen + oxycodone/ acetaminophen will provide greater relief of LBP than naproxen + cyclobenzaprine seven days after an ED visit, as measured by the Roland Morris low back pain functional disability scale
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Low Back Pain
Keywords
low back pain
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
323 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Opioid
Arm Type
Active Comparator
Arm Description
Naproxen + opioid
Arm Title
Skeletal muscle relaxant
Arm Type
Active Comparator
Arm Description
Naproxen + skeletal muscle relaxant
Arm Title
Naproxen alone
Arm Type
Active Comparator
Arm Description
Naproxen + placebo
Intervention Type
Drug
Intervention Name(s)
Naproxen
Intervention Description
Naproxen 500mg twice/ day x 10 days
Intervention Type
Drug
Intervention Name(s)
Cyclobenzaprine
Intervention Description
Cyclobenzaprine 5-10mg three times/ day x 10 days
Intervention Type
Drug
Intervention Name(s)
Oxycodone/ acetaminophen
Intervention Description
Oxycodone 5-10mg/ Acetaminophen 325-650 mg three times/ day x 10 days
Primary Outcome Measure Information:
Title
Change in Functional Disability as Measured by the Roland Morris Disability Questionnaire
Description
The Roland Morris Disability Questionnaire (RMDQ) is a 24 item instrument that evaluates the impact of low back pain on one's daily life. It is most sensitive for patients with mild to moderate disability due to acute, sub-acute or chronic low back pain. Each question can be answered as either a "yes" or "no". The score ranges from 0 to 24 where a higher score reflects greater impairment and, therefore, worsening in the quality of life. The change in RMDQ is obtained by subtracting the RMDQ score at one week after discharge from the baseline score.
Time Frame
Baseline and one week after discharge from emergency department
10. Eligibility
Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
64 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Non-radicular, non-traumatic low back pain of no more than 2 weeks duration
Exclusion Criteria:
Back pain longer than 2 weeks
Prior to the acute attack of low back pain, back pain once per month or more frequently
Prior to the acute attack of low back pain, daily or near daily use of pain medication
Facility Information:
Facility Name
Montefiore Medical Center
City
Bronx
State/Province
New York
ZIP/Postal Code
10467
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
26501533
Citation
Friedman BW, Dym AA, Davitt M, Holden L, Solorzano C, Esses D, Bijur PE, Gallagher EJ. Naproxen With Cyclobenzaprine, Oxycodone/Acetaminophen, or Placebo for Treating Acute Low Back Pain: A Randomized Clinical Trial. JAMA. 2015 Oct 20;314(15):1572-80. doi: 10.1001/jama.2015.13043.
Results Reference
derived
Learn more about this trial
A Randomized Study of Three Medication Regimens for Acute Low Back Pain
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