Study of the Insomnia in Patients With Low Back Pain
Primary Insomnia
About this trial
This is an interventional treatment trial for Primary Insomnia focused on measuring Insomnia, Low Back Pain, Hypnotics, Eszopiclone, Pain, Disability
Eligibility Criteria
Inclusion Criteria: • Diagnosis of insomnia based on DSM-IV criteria for insomnia due to a general medical condition (low-back pain); The insomnia must not predate the onset of low-back pain by more than 1 month; Usual nightly TST (Total Sleep Time) < 6.5 hours and/or usual SOL (Sleep Onset Latency) > 30 minutes for the last month prior to screening; ISI (Insomnia Severity Index) > 14 (at least moderate insomnia); Age 21-64 years; Greater than 40 on VAS (Visual Analog Scale) for pain (scale is 0-no pain to 100-worst imaginable pain); Patient Global Impression of Pain of at least 3 (on a 1-5 scale, indicating at least moderate severity); reported Back pain must be greater than reported leg pain, and there must be no signs of spinal nerve root compression; presence of normal motor strength on exam; duration of chronic low back pain of greater than three months; low back pain location must be inferior to T12 and superior to the gluteal fold. Exclusion Criteria: • Significant medical or neurological illness in excess of that which is directly responsible for the chronic low back pain; the presence of an active and significant psychiatric disease with a substantive impact on sleep; meeting DSM-IV criteria for an Axis I disorder within the last three months, or meeting criteria for substance abuse within the last 12 months; current pregnancy; history of hypersensitivity, intolerance, or contraindication to Naproxen/Lansoprazole or Eszopiclone; baseline creatinine of 2.0 or greater; patient taking other medications having significant renal effects (e.g. lithium, ACE inhibitor, angiotensin receptor antagonist, or thiazide/loop diuretics); patients taking other anticoagulants; patients having an allergy to aspirin; history of diagnosed gastric or duodenal ulcer; history of bleeding or clotting diathesis; lifetime history of myocardial infarction or cerebrovascular accident; Elevated PT/PTT/INR (Prothrombin Time, Partial Thromboplastin Time, International Normalized Ratio)at screening; Abnormal kidney function detected in screening labs; history of back related surgery within the past 3 months; history of corticosteroid use in the past 30 days; presence of currently pending litigation or worker's compensation claim related to the chronic low back pain; inability to follow study procedures or complete the study; or the use of any medications that could affect sleep within 5 half-lives of screening; history of back surgery within the past 2 years with the exception of a discectomy; pregnant or lactating females; women of child-bearing potential who will not agree to use approved means of birth control during the trial; history of any surgery within the past one month; history of any major physical trauma within the last 6 months; history of corticosteroid use within the last 90 days; diagnosis of rheumatoid or psoriatic arthritis; history of fibromyalgia; presence of spondyloarthropathy; presence of sciatica; spinal stenosis; presence of any vertebral fractures, spondylolisthesis; or radicular back pain.
Sites / Locations
- Duke University Medical Center
Arms of the Study
Arm 1
Arm 2
Placebo Comparator
Active Comparator
1
2
Placebo
Eszopiclone