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To determine the effects of pregabalin in reducing pain intensity and improving functional disability in patients with chronic low back pain of neuropathic origin when used in combination with Etoricoxib.
Hypothesis Pregabalin-etoricoxib combination is more effective than etoricoxib monotherapy in reducing pain and improving functional status in patients with chronic low back pain.
Null Hypothesis:
There is no significant difference between pregabalin-etoricoxib combination and etoricoxib monotherapy in reducing pain and improving functional status in patients with chronic low back pain.
Study Design: Comparative clinical study Setting: Watim General Hospital Duration of study: 18 months after ethical approval Sample Size: a previous study (8), was used to calculate the sample size, Using the WHO sample size calculator, a sample size of 140 patients (70 in each group) was determined with a 5% level of significance and 95% power of test.
Sampling Technique: non-probability convenience sampling. Sample selection
Inclusion criteria:
Exclusion Criteria:
Full description
Introduction When back pain persists for more than three months due to a variety of non-mechanical and mechanical diseases, it is considered chronic low back pain (CLBP) Fifty percent to eighty percent of the population will have chronic low back pain (CLBP) at some time in their lives. According to a study conducted in China in 2017 "global burden of disease", CLBP affects around 4.2% of those aged 20-29, and 19.6% of people aged 30-59. The global years lived with disability for LBP were 42.5 million in 1990, and increased 52.7% to 64.9 million in 2017. In addition to being the leading cause of requesting health care services, it is also associated with substantial impairment, treatment expenditures, and sick leave. This makes it all the more important to find effective methods of treating CLBP. Treatment of CLBP remains a clinical challenge for clinicians despite the availability of several pharmacologic and non-pharmacologic techniques. The failure to address the underlying cause of the pain is a major barrier to effective treatment of CLBP. Both the nociceptive and neuropathic pain (NeP) processes may be at play in chronic low back pain, making it a disorder with a wide range of possible causes. Analysis of a US claims database found that 90% of patients with CLBP have a neuropathic component. Neuropathic pain is generally associated with more severe pain symptoms. It is the result of multiple pathways at the peripheral, spinal, and supraspinal levels that trigger pain conduction pathway changes. When compared to individuals with no neuropathic pain component, those with CLBP incur an annual treatment cost that is almost 160% greater. Therefore, it is therapeutically crucial to differentiate between the nociceptive and neuropathic processes of CLBP and to treat this illness based on its underlying mechanisms in order to improve patient outcomes and reduce disease burden.
The majority of recommendations for treating Chronic LBP are non-pharmaceutical, including multidisciplinary rehabilitation, physical therapy, acupuncture, motor control exercise, mindfulness-based stress reduction, operant therapy, low-level laser therapy, cognitive behavioral therapy, or spinal surgery. However, in cases when the patient is unresponsive , treatment is started. Etoricoxib, is a highly selective cyclooxygenase-2 (COX-2) inhibitor with anti-inflammatory, analgesic, and antipyretic properties, recommended in the relief of acute and chronic pain , Indicated for pain and inflammation in osteoarthritis, in rheumatoid arthritis, in acute gouty arthritis, in chronic low back pain. Nonsteroidal anti-inflammatory drugs and simple analgesics, only work for nociceptive pain, have poor efficacy against NeP, and have the risk of side effects with long-term use , making the treatment of CLBP even more difficult when NeP is present.
Pregabalin and gabapentin are both derived from GABA, but they have no effect on the GABAergic system. Their mechanism of action includes binding to the alpha-2/delta-1 subunit of the voltage-gated calcium channels in several areas of the central nervous system (CNS) and spinal cord, and this is sufficient to explain their analgesic, anxiolytic, and anticonvulsant pharmacological properties. Voltage-gated calcium channels are localized on presynaptic terminals, where they control neurotransmitter release. Gabapentinoids, by binding to the alpha-2/ delta-1 subunit, destabilize the macromolecular complex that keeps the calcium channel on the surface of the presynaptic terminal, promoting its internalization.
46.5 percent of Pakistanis over the age of fifty have CLBP, according to recent estimates. There was a correlation between obesity, sedentary occupations, mental health issues, inactivity, ignorance about health risks, and heavy lifting in the Pakistani population, as shown by local statistics. The incidence of this condition is greater in cities than in rural regions. In Pakistan data shows that there are studies done on other uses of pregabalin, but its role in chronic low back pain is not known to be investigated.
Rationale:
The rationale of following study is to determine the role of pregabalin in chronic low back pain in order to address neuropathic component of pain.
Data collection Participants will be divided into two study groups. Group A (n=70) participant will receive 60mg Etoricoxib once daily along with a placebo and Group B (n=70) participants will also receive etoricoxib 60mg once daily(15) along with a placebo for 4 weeks. At the start of week 5 the group B will start taking Pregabalin 75mg along with Etoricoxib 60mg once daily for next 4 weeks, while, group A will continue same treatment as before. At Weeks 0 and 4 and 8 of the study, participants will be evaluated. Liver enzyme levels will be measured both at the beginning and end of the trial. The pain will be measured using numeric rating scale (NRS). It is an 11-point scale (a lower rating suggests improvement in back pain) 0 = no pain, 1-3 = mild pain, 4- 6 = moderate pain, 7-10 = worst/severe pain. CLBP-related impairment will be evaluated using the self-reported 24-item Roland-Morris impairment Questionnaire (RMDQ), which may be scored from 0 to 24. The bigger the score, the more severe the CLBP-related disability. Patient global impression of improvement is a global index used to rate the patients' impression of their condition's response to a specific treatment. The assessment is based on the following ratings: 1 = very much better, 2 = much better, 3 = a little better, 4 = no change, 5 = a little worse, 6 = much worse, 7 = very much worse. Assessments will be performed at week 8.
Data analysis Statistical analysis was performed using SPSS for Windows version 21. Descriptive analysis will be carried out and results will be presented in frequencies alongside means and standard deviation. The data will be tested for normality using the Kolmogorov-Smirnov statistic. Independent t-tests or their non-parametric analogues (Mann-Whitney U tests) will be used to compare group means. The change in values of the variables over time will be examined using ANOVA. The confounders will be accounted for using regression models. Quantitative information will be compared using the chi-squared test (or one tailed t-test). A significance level of ≤.05 will be used.
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Exclusion criteria
• Patients with the history of antidepressant, opioid, and benzodiazepine medications
Primary purpose
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140 participants in 2 patient groups
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Central trial contact
Eisha Akram, MBBS,MPhil
Data sourced from clinicaltrials.gov
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