A Randomized Study of Three Medication Regimens for Acute Low Back Pain

This study is currently recruiting participants.
Verified October 2012 by Montefiore Medical Center
Sponsor:
Information provided by (Responsible Party):
Benjamin Friedman, Montefiore Medical Center
ClinicalTrials.gov Identifier:
NCT01587274
First received: April 26, 2012
Last updated: October 27, 2012
Last verified: October 2012

April 26, 2012
October 27, 2012
April 2012
April 2014   (final data collection date for primary outcome measure)
Roland Morris low back pain functional disability scale [ Time Frame: 7 days after ER discharge ] [ Designated as safety issue: No ]
This questionnaire has 24 distinct questions which assess the impact of the low back pain on a patient's functionality
Same as current
Complete list of historical versions of study NCT01587274 on ClinicalTrials.gov Archive Site
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A Randomized Study of Three Medication Regimens for Acute Low Back Pain
A Randomized Three-armed Comparative Effectiveness Study of Various Medications for Musculoskeletal Low Back Pain: Defining the Added Benefit of Muscle Relaxants and Opioids.

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:

  1. 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
  2. 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
  3. 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
Not Provided
Interventional
Phase 4
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Acute Low Back Pain
  • Drug: Naproxen
    Naproxen 500mg twice/ day x 10 days
  • Drug: Cyclobenzaprine
    Cyclobenzaprine 5-10mg three times/ day x 10 days
  • Drug: Oxycodone/ acetaminophen
    Oxycodone 5-10mg/ Acetaminophen 325-650 mg three times/ day x 10 days
  • Active Comparator: Opioid
    Naproxen + opioid
    Interventions:
    • Drug: Naproxen
    • Drug: Oxycodone/ acetaminophen
  • Active Comparator: Skeletal muscle relaxant
    Naproxen + skeletal muscle relaxant
    Interventions:
    • Drug: Naproxen
    • Drug: Cyclobenzaprine
  • Active Comparator: Naproxen alone
    Naproxen + placebo
    Intervention: Drug: Naproxen
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
323
August 2014
April 2014   (final data collection date for primary outcome measure)

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
Both
21 Years to 64 Years
No
Not Provided
United States
 
NCT01587274
Low Back Pain RCT
Yes
Benjamin Friedman, Montefiore Medical Center
Montefiore Medical Center
Not Provided
Not Provided
Montefiore Medical Center
October 2012

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