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临床试验/NCT06424041
NCT06424041Enrolling By Invitation2 期

Fecal Microbiome Transplantation From Healthy Donors to Individuals With Fibromyalgia: A Prospective Randomized, Controlled Double-Blind Study

Rambam Health Care Campus2 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2024年3月11日最近更新:
适应症

试验速览

阶段
2 期
状态
Enrolling By Invitation
入组人数
100
试验地点
2
主要终点
Pain intensity at week five post-transplantation

研究概览

简要总结

This study aims to investigate if a fecal microbiome transplantation (FMT) from healthy donors can reduce symptoms of fibromyalgia, a condition causing chronic pain that is difficult to treat and diagnose. Changes in the gut bacteria of women with fibromyalgia were previously reported, which might be linked to their symptoms. In mice studies, transferring gut bacteria from individuals with fibromyalgia was shown to increase sensitivity to pain, while treatment with antibiotics and transferring bacteria from healthy individuals reversed this effect. In a small open label trial in women, improvements in pain, fatigue, and sleep problems were observed after FMT. The investigators aim to perform a larger trial following a similar path. The study aims to conduct a double-blinded, randomized, placebo-controlled trial involving 80 women diagnosed with severe fibromyalgia. Half of the participants (40) will receive the active treatment, while the other half (40) will receive a sham treatment. The allocation to either group will be randomized. Throughout the study period, both the caregivers and the participants will remain unaware of their assigned groups until the study conclusion. Participants' symptoms will be documented and their blood and stool will be tested for changes in certain metabolites. If this treatment works, it could be a significant breakthrough in managing fibromyalgia and might provide new insights into its causes.

详细描述

A double-blind, randomized placebo-controlled study to test the therapeutic potential of encapsulated oral fecal microbiota transplantation (FMT) from healthy donors to humans with fibromyalgia.

Fibromyalgia, a chronic and debilitating syndrome characterized by widespread pain, fatigue, sleep disturbances, and cognitive dysfunction poses a significant clinical, social, and economic burden globally, with limited targeted treatment options available. Recent studies have shed light on the potential role of the gut microbiome in fibromyalgia pathogenesis, highlighting alterations in gut microbiome composition correlated with clinical indices of the syndrome. Building upon this knowledge, the study seeks to explore the therapeutic potential of FMT, a well-established treatment increasingly investigated across various medical conditions. Preclinical investigations in mice have shown that FMT from fibromyalgia patients induces symptoms of the syndrome, while FMT from healthy controls reverses them. Encouragingly, preliminary results from an open-label pilot clinical trial involving fibromyalgia patients receiving encapsulated oral FMT from healthy donors demonstrated significant improvements in pain intensity, symptomatic burden, and quality of life measures, with favorable safety profiles. Based on these promising findings, a prospective randomized, controlled double-blind study is proposed to further evaluate the efficacy and safety of encapsulated oral FMT from healthy individuals in fibromyalgia patients. Clinical outcomes, as well as stool and serum samples, will be extensively characterized to elucidate the mechanisms underlying the effects of FMT, including its modulation of gut microbiome composition and function. The hypotheses involve expecting clinically significant improvements in pain and other symptoms of fibromyalgia following FMT, alongside corresponding alterations in gut microbiome composition and metabolomics profiles. This study aims to contribute valuable insights into the potential role of FMT as a novel therapeutic approach for fibromyalgia, addressing an unmet need in the management of this challenging condition.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Adult women aged 18-75 years.
  • Diagnosis of fibromyalgia confirmed according to the 2016 diagnostic criteria by a pain physician who is a part of the study team.
  • An average reported pain of 6 or above during the preceding week.
  • Has remained symptomatic despite receiving standard care for fibromyalgia.

排除标准

  • Any active inflammatory condition (rheumatic, gastrointestinal or other).
  • Malignant neoplasm in the preceding 5 years.
  • Immunosuppression due to medical condition or treatment.
  • Uncontrolled psychiatric pathology.
  • Any other clinically important condition at the discretion of the investigator.
  • Known allergy to the antibiotics or laxatives used in the preparation protocol, or severe food allergy.
  • Active infection or expected antibiotic treatment in the upcoming 3 months after inclusion.
  • Pregnancy or intention to conceive.

结局指标

主要结局

Pain intensity at week five post-transplantation

时间窗: Week five post transplantation induction

Pain intensity will be assessed using the Visual Analogue Scale (VAS), with a score of zero indicating no pain and a score of 10 representing the worst possible pain.

次要结局

  • Sleep quality(Week five post transplantation induction and then on months 1, 3, 6 after last FMT)
  • Quantitative Sensory Testing(Week five post transplantation induction and then on months 1, 3, 6 after last FMT)
  • overall symptomatic burden(Week five post transplantation induction and then on months 1, 3, 6 after last FMT)
  • Anxiety and depression(Week five post transplantation induction and then on months 1, 3, 6 after last FMT)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Amir Minerbi MD

Deputy Director

Rambam Health Care Campus

研究点 (2)

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