The effectiveness of pregabalin with or without agomelatine in the treatment of chronic low back pain: a double-blind, placebo-controlled, randomized clinical trial

被引:3
|
作者
Mahdavi, Seyed Mani [1 ]
Shariati, Behnam [2 ]
Shalbafan, Mohammadreza [2 ]
Rashedi, Vahid [3 ]
Yarahmadi, Masoomeh [4 ]
Ghaznavi, Alireza [1 ]
Amiri, Shayan [1 ]
机构
[1] Iran Univ Med Sci, Bone & Joint Reconstruct Res Ctr, Sch Med, Dept Orthoped, Tehran, Iran
[2] Iran Univ Med Sci, Mental Hlth Res Ctr, Sch Med, Dept Psychiat,Psychosocial Hlth Res Inst PHRI, Tehran, Iran
[3] Univ Social Welf & Rehabil Sci, Iranian Res Ctr Aging, Dept Aging, Tehran, Iran
[4] Iran Univ Med Sci, Sch Behav Sci & Mental Hlth, Tehran, Iran
来源
BMC PHARMACOLOGY & TOXICOLOGY | 2022年 / 23卷 / 01期
关键词
Low back pain; Agomelatin; Pregabalin; Clinical trial; NEUROPATHIC PAIN; VALIDATION; FIBROMYALGIA; TRANSLATION; COMPONENTS; CARE;
D O I
10.1186/s40360-022-00612-3
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background Although various pharmacological and nonpharmacological treatments are available for the chronic low back pain (CLBP), there is no consensus on the best optimal treatment for this condition. This study aimed to investigate the efficacy of co-administration of pregabalin and agomelatine versus pregabalin with placebo to treat CLBP. Methods Forty-six CLBP patients without the surgical indication referred to the outpatient orthopedic clinic of Rasoul-e-Akram Hospital, Tehran, Iran, were randomly divided into two study groups: Group A [pregabalin (75 mg twice per day) + placebo] and Group B [pregabalin (75 mg twice per day) + agomelatine (25 mg per night)]. Patients were evaluated at weeks 0, 4, and 8. Outcome measures were the Persian versions of the Brief Pain Inventory (BPI) interference scale, Roland-Morris Disability Questionnaire (RMDQ), The Hospital Anxiety and Depression Scale (HADS), 36-Item Short Form Survey (SF-36), and General Health Questionnaire-28 (GHQ-28) were used. Results At weeks 4 and 8 after the intervention, all evaluated measures showed significant improvement in both study groups (P < 0.01). The mean improvement of GHQ-28 was 3.7 +/- 1.22 in group A and 13.1 +/- 4.71 in group B. This difference was statistically significant (P = 0.003). Other outcomes did not vary substantially between the two research groups. Agomelatine treatment was well tolerated, with no significant adverse effects seen in patients. Liver tests of all patients were routine during the study period. Major adverse effect was not seen in any patient. The prevalence of Minor side effects was not significantly different between two study groups. Conclusion Compared with the pregabalin and placebo, co-administration of pregabalin and agomelatine had no added effect on improving pain scores in CLBP patients. However, the patients' general health was significantly improved after the combined administration of pregabalin and agomelatine.
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页数:8
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