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临床试验/CTRI/2019/11/021918
CTRI/2019/11/021918已完成2 期

Efficacy of individualized homeopathic medicines in treatment of lumbar spondylosis: Double-blind, randomized, placebo-controlled clinical trial

National Institute of Homoeopathy1 个研究点 分布在 1 个国家目标入组 66 人开始时间: 2019年11月18日最近更新:

试验速览

阶段
2 期
状态
已完成
入组人数
66
试验地点
1
主要终点
Oswestry low back pain questionnaire

研究概览

简要总结

Lumbar spondylosis (LS) is a degenerative disorder of the lumbar spine. Despite substantial research efforts, no gold-standard treatment for LS has been identified. The efficacy of individualized homeopathic medicines (IHMs) in LS has remained under-researched. In this study, the efficacy of IHMs was compared with identical-looking placebos in the treatment of LS. A double-blind, randomized (1:1), placebo-controlled trial was conducted at the National Institute of Homoeopathy, West Bengal, India. Patients were randomized to receive IHMs or identical-looking placebos, along with standardized concomitant care for both the groups. The Oswestry low back pain and disability questionnaire (ODQ) was the primary outcome; the Roland Morris questionnaire (RMQ) and the short form McGill pain questionnaire (SF-MPQ) were the secondary outcomes; each was measured at baseline and every month for 3 months. The intention-to-treat (ITT) sample was analyzed to detect any inter-group differences using two-ways repeated measures analysis of variance models overall and by unpaired t-tests at different time points. Enrolment was stopped prematurely because of time restrictions; 55 patients were randomized (verum: 28; control: 27); 49 were analyzed by ITT (verum: 26; control: 23). Inter-group differences in ODQ, RMQ and SF-MPQ total scores at 3 months were not statistically significant. SF-MPQ total score after 2 months revealed statistical significance, favoring IHMs against placebos. Some of the SF-MPQ subscales at different time points were also significant. Rhus toxicodendron, Sulphur and Pulsatilla nigricans were the most frequently indicated medicines. Owing to failure in detecting a statistically significant effect for the primary outcome and in recruiting a sufficient number of participants, our trial remained inconclusive.

研究设计

研究类型
Interventional
分配方式
Permuted block randomization, variable
盲法
Participant, Investigator and Outcome Assessor Blinded

入排标准

年龄范围
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • Patients with radiological diagnosis of lumbar spondylosis with mild to moderate degenerative radiological changes
  • Patients of age 18 to 65 years
  • Patients of both sexes
  • Literate patients, able to read and write in Bengali
  • Patients giving written consent to participate.

排除标准

  • Patients having severe degenerative changes as found in radiological findings
  • Patients having major disorder associated with lumbar spondylosis
  • Patients undergoing homeopathic treatment for any chronic disease within last 3 months.
  • Diagnosed cases of unstable mental or psychiatric illness or other uncontrolled or life.
  • threatening illness affecting quality of life or any organ failure
  • Pregnancy and lactation
  • Substance abuse and/or dependence
  • Self-reported immune-compromised state.

结局指标

主要结局

Oswestry low back pain questionnaire

时间窗: At baseline, and every month, up to 3 months

次要结局

  • Roland Morris questionnaire(At baseline, and every month, up to 3 months)
  • McGill pain questionnaire short form (SF-MPQ)(At baseline, and every month, up to 3 months)

研究者

申办方类型
Government medical college

研究点 (1)

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