Cipralex in Treatment of Depressive Symptoms and Chronic Back Pain

Condition(s) targeted: Low Back Pain; Depression

Intervention: Escitalopram (Drug); Placebo (Drug)

Phase: Phase 4

Status: Recruiting

Sponsored by: Martin-Luther-Universität Halle-Wittenberg

Official(s) and/or principal investigator(s):
Ulrich W Preuss, MD, Principal Investigator, Affiliation: Krankenhaus Bethanien gGmbH

Overall contact:
Ulrich W Preuss, MD, Phone: +49345557, Ext: 4595, Email: ulrich_preuss@hotmail.com

Chronic low back pain (CLBP) is one of the most frequent forms of chronic pain and can result in significant functional impairment. This is often associated with major depression too. Previous research reported significant beneficial effects of antidepressant medication in alleviating depression and pain intensity. The aim of this study is to evaluate the efficacy of Escitalopram, a new kind of Selective Serotonin Reuptake Inhibitor (SSRI) in patients with CLBP in a prospective, randomized and double-blind clinical trial. The main hypothesis is:

- in comparison to placebo, subjects with CLBP and Cipralex report a significant reduction in

depressive symptoms (>= 50% of HAMD questionnaire) after 4 weeks of treatment.

Official title: Cipralex in Treatment of Depressive Symptoms and Chronic Back Pain

Study design: Treatment, Randomized, Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Placebo Control, Parallel Assignment, Efficacy Study

Primary outcome: In comparison to placebo-treated patients, patients with treated with Cipralex report a significant reduction in depressive symptoms (>= 50% HAMD score) after 4 weeks of treatment.

Secondary outcome:

In comparison to placebo, subjects treated with Cipralex report a significant reduction in pain intensity (>= 50% reduction of pain questionnaire score or VAS) after 12 weeks of treatment.

In comparison with placebo, subjects treated with Cipralex report a significant improvement in physical and everyday functioning after 12 weeks of treatment.

Personality traits do not have a significant influence on outcome regarding depressive traits, pain intensity and functioning.

Personality disorders are significantly influencing worse outcome regarding depressive traits, pain intensity and functioning.

Detailed description: Pain is an unpleasant sensory and emotional experience. Chronic pain, including chronic low back pain, represents a major public health problem. Risk factors of chronicity of low back pain include high levels of psychological distress prior to or during the episode, premorbid association with work status or employment dissatisfaction, unemployment, poor self-rated health and low levels of physical activity. Other psychosocial features are poor social and educational status, previous sexual or physical abuse. Furthermore, mechanical strain on the spine from heavy lifting, repetitive lifting, twisting and vibration, including driving increase the risk. Static work postures, prolonged standing or walking, road traffic accidents and falls are also significantly related. While there is little evidence for a specific personality profile, stress, distress, anxiety, mood disorders and depression were consistently related to neck and back pain.

CLBP is associated with significant disability, functional impairment, high rates of psychiatric symptoms including anxiety and depression, and loss of other physical roles. These may produce social and functional problems, which include reduced earning capacity, unemployment and family disharmony. Chronic pain is also associated with loss of self confidence and self-esteem, leading to social withdrawal and social isolation. Men with CLBP have significantly higher lifetime rates of major depression, alcohol use disorder and major anxiety disorder. After age of pain onset, CLBP subjects had over 9 times the risk of developing major depression.

Depression is believed to be mediated by 5-HT and norepinephrine through the raphe nucleus and locus coeruleus projections to the cerebral cortex and forebrain limbic systems, whereas pain is believed to be mediated in part through descending 5-HT and norepinephrine pain pathways that provide inhibitory input to the dorsal horn neurons in the spinal cord. Global deficiences in 5-HT or norepinephrine neurotransmission would be predicted to affect both mood and pain thresholds, possibly accounting for the hgh comorbidity of painful symptoms in patients with depression. Accordingly, enhancement of both neurotransmitter or 5-HT alone would be expected both to improve symptoms of depression and to normalize pain thresholds.

In antidepressant treatment of CLBP, only 2 studies were published using SSRIs. One reported significantly higher pain intensity reduction in maprotilin group compared to paroxetine and placebo. The other showed no effect of paroxetine on depression or pain. Patients on SSRI, however, reduced the amount of analgesic medication.

Minimum age: 18 Years. Maximum age: 65 Years. Gender(s): Both.

Criteria:

Inclusion Criteria:

- In- and out-patients at KH Bethanien, Greifswald, presenting with non-specific chronic

low back pain lasting longer than 6 months (assessed with VAS and OLBPQ rev.)

- Age from 18 to 65 years

- Depressive symptoms (HAMD scores >10)

- Significant disability in daily living tasks (Owestry Disability Index >30%)

- Medication with nonsteroidal anti-inflammatory drugs.

Exclusion Criteria:

- Other significant Axis I disorders, including psychosis, eating disorders, substance

use disorders or recent suicidal behavior.

- Systemic inflammatory disorder, malignancy, other acute medical or neurological

disorders, recent surgery within 12 months.

- Medication with opioids, corticosteroids, other psychotropic medication except

Temazepam.

- History of gastric ulcer, gastritis or gastric bleeding.

- Known allergy or intolerance to Citalopram or Cipralex.

- Pregnant or lactating women.

Ulrich W Preuss, MD, Phone: +49345557, Ext: 4595, Email: ulrich_preuss@hotmail.com

Martin-Luther-University Halle, Halle, Sachsen-Anhalt 06097, Germany; Recruiting
Ulrich W Preuss, MD, Phone: +49345557, Ext: 4595, Email: ulrich_preuss@hotmail.com
Jessica Wong, MD, Phone: +493456922, Ext: 145, Email: wong_preuss@hotmail.com
Ulrich W. Preuss, MD, Principal Investigator

Starting date: November 2007
Ending date: November 2010
Last updated: July 3, 2008