Migu Capsules in the Treatment of Osteoporotic Low Back Pain in Postmenopausal Women: A Single-Center Randomized Controlled Trial.

IF 2.5 3区 医学 Q2 CLINICAL NEUROLOGY Journal of Pain Research Pub Date : 2024-12-31 eCollection Date: 2024-01-01 DOI:10.2147/JPR.S477969
Chen-Ming Tang, Yuan-Chuan Chen, Yu-Cheng Huang, Yuan Meng, Jing-Chun Xia, Jian Pang, Ying Shi
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Abstract

Purpose: This trial aimed to investigate the efficacy of Migu capsules in treating osteoporotic low back pain.

Patients and methods: In this single-center trial, we randomly assigned patients with osteoporotic low back pain that had lasted for 3 months in a 1:1 ratio to receive Migu capsules alongside Caltrate D in treatment group or to receive Caltrate D only in control group, both for 48 weeks. The primary outcome measure was the intensity of low back pain on a visual analog scale at 24 weeks after enrollment. Secondary outcome measures included the Roland-Morris Disability Questionnaire (RMDQ), bone turnover markers, and bone mineral density.

Results: A total of 100 patients were enrolled, with 50 in each group. At baseline, the mean score for low back pain intensity was 6.2 in the treatment group and 6.1 in the control group. The primary outcome of the low back pain intensity score at 24 weeks was 2.9 in the treatment group and 4.7 in the control group (adjusted mean difference, -1.8; 95% confidence interval, -2.3 to -1.4; P<0.001). Secondary outcomes including the score on RMDQ and pain at 48 weeks were in the same direction as the primary outcome. Compared to the control group, the treatment group only showed a difference in bone density after continuous intervention for 48 weeks (P<0.05). Three patients experienced a mild adverse event associated with the intake of Migu capsules.

Conclusion: Migu capsules can alleviate bone pain and reduce functional disabilities caused by osteoporotic lower back pain.

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咪骨胶囊治疗绝经后妇女骨质疏松性腰痛:一项单中心随机对照试验
目的:观察咪骨胶囊治疗骨质疏松性腰痛的疗效。患者和方法:在本单中心试验中,我们将持续3个月的骨质疏松性腰痛患者按1:1的比例随机分配给治疗组服用咪骨胶囊并服用钙D或对照组只服用钙D,疗程均为48周。主要结果测量是在入组后24周的视觉模拟量表上腰痛的强度。次要结局指标包括罗兰-莫里斯残疾问卷(RMDQ)、骨转换标志物和骨矿物质密度。结果:共入组患者100例,每组50例。基线时,治疗组腰痛强度平均评分为6.2,对照组为6.1。24周时腰痛强度评分的主要终点,治疗组为2.9分,对照组为4.7分(校正平均差为-1.8;95%置信区间为-2.3 ~ -1.4;结论:咪骨胶囊可减轻骨质疏松性腰痛所致的骨痛和功能障碍。
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来源期刊
Journal of Pain Research
Journal of Pain Research CLINICAL NEUROLOGY-
CiteScore
4.50
自引率
3.70%
发文量
411
审稿时长
16 weeks
期刊介绍: Journal of Pain Research is an international, peer-reviewed, open access journal that welcomes laboratory and clinical findings in the fields of pain research and the prevention and management of pain. Original research, reviews, symposium reports, hypothesis formation and commentaries are all considered for publication. Additionally, the journal now welcomes the submission of pain-policy-related editorials and commentaries, particularly in regard to ethical, regulatory, forensic, and other legal issues in pain medicine, and to the education of pain practitioners and researchers.
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