The Effect of Pregabalin and Etoricoxib on Pain Alone Versus in Combination
NCT ID: NCT06401499
Last Updated: 2024-05-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
NOT_YET_RECRUITING
PHASE4
140 participants
INTERVENTIONAL
2024-06-01
2024-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
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:
* Participants within age 20-65 years
* Both male and non-pregnant non-lactating female patients will be included in the study
* Patients experiencing CLBP symptoms from last 6 months
* No experience of previous low back surgery
Exclusion Criteria:
* Patients with the history of antidepressant, opioid, and benzodiazepine medications
* Patients with the history of CYP1A2 inhibitors usage
* Patients already taking pregabalin
* Patients with the history of suicidal ideation, severe depression, anxiety disorder psychosis, and cognitive impairment 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). CLBP-related impairment will be evaluated using the self-reported 24-item Roland-Morris impairment Questionnaire (RMDQ)
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
PROs in Chronic Low Back Pain Patients With Accompanying Lower Limb Pain (Neuropathic Component) Treated With Pregabalin
NCT02273908
Study of Pregabalin in the Prevention of Central Neuropathic Pain in Acute Spinal Cord Injury
NCT00879021
An Investigation of the Effects of Erythromycin on the Pharmacokinetics of the Pregabalin Controlled Release Tablet
NCT01342198
Pain Prevention and Treatment Through the Enhancement of the Anti-nociceptive Component of Pain Modulation Profiles
NCT02020122
A Study of the Efficacy and Safety of Pregabalin for the Treatment of Fibromyalgia
NCT00645398
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
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.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
etoricoxib 60mg
tablet etoricoxib 60mg once daily for four weeks
etoricoxib 60mg
investigator will compare effects of etoricoxib alone and in combination with pregabalin on pain relief in chronic low back pain participants
pregabalin 75mg
tablet pregabalin 75mg once daily for 4 weeks tablet etoricoxib 60mg once daily for four weeks
etoricoxib 60mg
investigator will compare effects of etoricoxib alone and in combination with pregabalin on pain relief in chronic low back pain participants
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
etoricoxib 60mg
investigator will compare effects of etoricoxib alone and in combination with pregabalin on pain relief in chronic low back pain participants
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Both male and non-pregnant non-lactating female patients will be included in the study
* Patients experiencing CLBP symptoms from last 6 months
Exclusion Criteria
* Patients with the history of CYP1A2 inhibitors usage
* Patients already taking pregabalin
* Patients with the history of suicidal ideation, severe depression, anxiety disorder psychosis, and cognitive impairment
20 Years
65 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Muhammad Ilyas
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Muhammad Ilyas
senior lecturer
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
References
Explore related publications, articles, or registry entries linked to this study.
Allegri M, Montella S, Salici F, Valente A, Marchesini M, Compagnone C, Baciarello M, Manferdini ME, Fanelli G. Mechanisms of low back pain: a guide for diagnosis and therapy. F1000Res. 2016 Jun 28;5:F1000 Faculty Rev-1530. doi: 10.12688/f1000research.8105.2. eCollection 2016.
Fatoye F, Gebrye T, Odeyemi I. Real-world incidence and prevalence of low back pain using routinely collected data. Rheumatol Int. 2019 Apr;39(4):619-626. doi: 10.1007/s00296-019-04273-0. Epub 2019 Mar 8.
Wu A, March L, Zheng X, Huang J, Wang X, Zhao J, Blyth FM, Smith E, Buchbinder R, Hoy D. Global low back pain prevalence and years lived with disability from 1990 to 2017: estimates from the Global Burden of Disease Study 2017. Ann Transl Med. 2020 Mar;8(6):299. doi: 10.21037/atm.2020.02.175.
Meucci RD, Fassa AG, Faria NM. Prevalence of chronic low back pain: systematic review. Rev Saude Publica. 2015;49:1. doi: 10.1590/S0034-8910.2015049005874. Epub 2015 Oct 20.
Sakai Y, Ito K, Hida T, Ito S, Harada A. Neuropathic pain in elderly patients with chronic low back painand effects of pregabalin: a preliminary study. Asian Spine J. 2015 Apr;9(2):254-62. doi: 10.4184/asj.2015.9.2.254. Epub 2015 Apr 15.
Yeole AB, Sree Ranga Lakshmi G, Selvakumar CJ, Goni VG, Nawal CL, Valya BJ, Patel BJ, Patel RD, Pawar ED, Panigrahi R, Kumar AY, Shintre SS, Devkare PH, Dharmadhikari SK, Choudhari SY, Doshi MS, Mehta SC, Joglekar SJ. Efficacy and Safety of Pregabalin Prolonged Release-Etoricoxib Combination Compared to Etoricoxib for Chronic Low Back Pain: Phase 3, Randomized Study. Pain Ther. 2022 Dec;11(4):1451-1469. doi: 10.1007/s40122-022-00437-2. Epub 2022 Oct 12.
Caglar Okur S, Vural M, Pekin Dogan Y, Mert M, Sayiner Caglar N. The effect of pregabalin treatment on balance and gait in patients with chronic low back pain: a retrospective observational study. J Drug Assess. 2019 Feb 4;8(1):32-35. doi: 10.1080/21556660.2019.1579098. eCollection 2019.
Otto JC, Forstenpointner J, Sachau J, Hullemann P, Hukauf M, Keller T, Gierthmuhlen J, Baron R. A Novel Algorithm to Identify Predictors of Treatment Response: Tapentadol Monotherapy or Tapentadol/Pregabalin Combination Therapy in Chronic Low Back Pain? Front Neurol. 2019 Sep 13;10:979. doi: 10.3389/fneur.2019.00979. eCollection 2019.
Igarashi A, Akazawa M, Murata T, Taguchi T, Sadosky A, Ebata N, Willke R, Fujii K, Doherty J, Kobayashi M. Cost-effectiveness analysis of pregabalin for treatment of chronic low back pain in patients with accompanying lower limb pain (neuropathic component) in Japan. Clinicoecon Outcomes Res. 2015 Oct 7;7:505-20. doi: 10.2147/CEOR.S89833. eCollection 2015.
Fornasari D. Pharmacotherapy for Neuropathic Pain: A Review. Pain Ther. 2017 Dec;6(Suppl 1):25-33. doi: 10.1007/s40122-017-0091-4. Epub 2017 Nov 24.
Mathieson S, Lin CC, Underwood M, Eldabe S. Pregabalin and gabapentin for pain. BMJ. 2020 Apr 28;369:m1315. doi: 10.1136/bmj.m1315. No abstract available.
Taguchi T, Nakano S, Nozawa K. Effectiveness of Pregabalin Treatment for Neuropathic Pain in Patients with Spine Diseases: A Pooled Analysis of Two Multicenter Observational Studies in Japan. J Pain Res. 2021 Mar 16;14:757-771. doi: 10.2147/JPR.S293556. eCollection 2021.
Siddiqui AS, Javed S, Abbasi S, Baig T, Afshan G. Association Between Low Back Pain and Body Mass Index in Pakistani Population: Analysis of the Software Bank Data. Cureus. 2022 Mar 30;14(3):e23645. doi: 10.7759/cureus.23645. eCollection 2022 Mar.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
WM&DCR/R&D(ERB)/2024/92
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.