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FMT for MS Patients (MS-FMT)

2022년 10월 24일 업데이트: Michael Silverman, MD, Lawson Health Research Institute

Fecal Microbial Transplantation for Relapsing Multiple Sclerosis Patients - a Placebo-controlled, Double-blinded, Randomized Trial

This is a placebo-controlled, double-blinded, randomized trial design, whereby all patients are eligible to start an injectable therapy, and then randomized to either placebo or FMT for approximately 1 year.

연구 개요

상세 설명

Fecal Microbiome Transplants: Patients will undergo pretreatment with Amoxicillin/Clavulinate (or matched placebo) for 5 days followed by a bowel cleanse with PEGLYTE. Patients will undergo allogeneic or autologous fecal transplants. Patients will be dosed with FMT oral capsules approximately 48 hours after antibiotic treatment has stopped. Following the FMT capsule treatment on day 1, patients will be administered a repeat oral capsule or placebo dose at 3 weeks. Oral omeprazole or omeprazole placebo will be given 1 hour prior to the baseline and 3 week dose. This will be done to ensure full engraftment of the transplant.

Participants will be seen at baseline, 3 weeks, 6 weeks, 3 months, 6 months and 12 months. A series of neurological tests will be performed for safety measures. In addition to this, MRIs will be completed at baseline, 6 weeks and 12 months. Blood, urine and stool samples will also be collected for data analysis and safety measures.

연구 유형

중재적

등록 (예상)

34

단계

  • 2 단계

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

18년 (성인)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

설명

Inclusion Criteria:

  • 18 - 55 years of age
  • Have an expanded disability status scale (EDSS) of < 6
  • Have a diagnosis of relapsing multiple sclerosis
  • Have evidence of radiographic activity within the 12 months on MRI (new/enlarging T2 lesion or gadolinium enhancing lesion)
  • Eligible to start/starting an injectable DMT
  • Not on a DMT currently and/or not on a DMT in last 6 months
  • Ability to swallow capsules

Exclusion Criteria:

  • Unable to provide informed consent
  • Does not pass the standard MRI screening questionnaire
  • Other disease that can affect GI permeability (such as Inflammatory Bowel Disease, Crohn's disease, ulcerative colitis, indeterminate colitis or microscopic colitis, celiac disease)
  • Expected requirement for antibiotics within 3 months (chronic suppressive therapies, elective prosthetic joint insertion)
  • Toxic megacolon, small bowel ileus
  • Penicillin allergy
  • Omeprazole allergy

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 기초 과학
  • 할당: 무작위
  • 중재 모델: 병렬 할당
  • 마스킹: 더블

무기와 개입

참가자 그룹 / 팔
개입 / 치료
위약 비교기: Autologous Transplants
Healthy donor stool will be processed and placed into capsules.
Participants stool will be processed and placed into capsules.
활성 비교기: Allogeneic Transplants
Healthy donor stool will be processed and placed into capsules.
Participants stool will be processed and placed into capsules.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Changes in T2 Lesions - MRI
기간: Baseline, 6 weeks, 12 months
Assess the number of new/enlarging/gad enhancing T2 lesions. We will be comparing baseline to 6 weeks and 6 weeks to 12 months.
Baseline, 6 weeks, 12 months

2차 결과 측정

결과 측정
측정값 설명
기간
Blood Brain Barrier - MRI
기간: Baseline, 6 weeks, 12 months
We will assess the integrity of the blood brain barrier through MRI from baseline to 6 weeks and 6 weeks to 12 months.
Baseline, 6 weeks, 12 months
Neurofilament Light Serum Levels
기간: Baseline, 6 weeks, 3 months, 12 months

As a biomarker of neuronal damage neurofilament light chain levels will be detected. Peripheral blood will be collected in appropriate tubes at baseline, 6 weeks, 3 months and 12 months and processed for serum.

Once collected all samples will be sent to the University of Ottawa where a Simoa NfL assay will be undertaken on their Simoa Analyzer.

Patients with multiple sclerosis have been shown to have increased intestinal permeability, likely due to a reduction in butyrate-producing bacteria. A decrease in butyrate producing bacteria has been shown to be associated with increased intestinal permeability. Relapsing-remitting MS patients have been shown to have increased intestinal permeability, which may allow dietary and microbial antigens from the intestinal lumen to pass into the blood stream and cause autoimmune responses in MS patients. This may prime the immune system to develop a humoral response to certain bacteria.

Baseline, 6 weeks, 3 months, 12 months
Intestinal Permeability
기간: Baseline, 6 weeks, 12 months
Small Intestine Permeability: Mannitol/Lactulose administration will be used and urine will be collected to measure small intestine permeability. For small intestine permeability patients will be instructed to drink lactulose solution and collect the urine throughout the night and first thing in the morning. A proper collecting bottle will be provided. Once the urine sample bottle reaches the laboratory University Hospital the total volume will be measured and an aliquot of 30mL total, 10mL in each sterile urine container (no other additives) will be separated and stored at -20C and sent on dry ice to Dr. Meddings laboratory at Calgary, Alberta. All biological material will be transported according to biosafety regulations.
Baseline, 6 weeks, 12 months
IgA Microbiota
기간: Baseline, 3 weeks, 6 weeks, and 12 months
IgA Microbiota analysis: IgA bound bacteria will be detected and sorted (magnetic beads or flow cytometry) using anti-IgA (pan-IgA, detect monomer and secreted multimer (Miltenyi clone: IS11-8E10). Sorted IgA bound bacteria will be stored, and the DNA extracted in one batch at the end of the study. Changes in the composition of IgA bound bacteria for each patient will be determined using the previously mentioned methods. (Rojas, et al. 2018; Planer, et al. 2016)
Baseline, 3 weeks, 6 weeks, and 12 months
Stool Microbiome
기간: Baseline, 3 weeks, 6 weeks, 3 months, 6 months, 12 months
Gut microbiota analysis before and after FMT: Toilet paper samples will be collected from patients' at baseline and 1-2 days before each scheduled appointment (Al et al. 2018). Patients will store the toilet paper inside of DNA free plastic bags and keep them at 4 °C in the refrigerator until the time of their appointment (alternatively, the samples can be mailed in to the lab, but one method must be chosen for all of the samples collected). Toilet paper samples will be collected from the FMT donor every time they drop off a stool sample for donation. DNA from the toilet paper samples will be extracted in one batch at the end of the study and sent for Illumina Mi-Seq next-generation sequencing of the V4 region of the 16S rRNA gene. Changes in the composition of gut bacteria will be determined using custom R scripts.
Baseline, 3 weeks, 6 weeks, 3 months, 6 months, 12 months
Metabolomics
기간: Baseline, 3 weeks, 6 weeks, 3 months, 6 months, 12 months
Metabolomics: Serum will be collected for metabolomic analysis. Metabolomics can be used to identify biomarkers of MS and may provide us with information about which patients are more likely to respond to FMT therapy. Butyrate producing bacteria have been shown to be in lower relative abundance in MS patients and concentrations of short-chain fatty acids in stool and will be investigated before and after FMT.
Baseline, 3 weeks, 6 weeks, 3 months, 6 months, 12 months
Metabolomics
기간: Baseline, 3 weeks, 6 weeks, 3 months, 6 months, 12 months
Metabolomics: Urine will be collected for metabolomic analysis. Metabolomics can be used to identify biomarkers of MS and may provide us with information about which patients are more likely to respond to FMT therapy. Butyrate producing bacteria have been shown to be in lower relative abundance in MS patients and concentrations of short-chain fatty acids in stool and will be investigated before and after FMT.
Baseline, 3 weeks, 6 weeks, 3 months, 6 months, 12 months

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (예상)

2023년 6월 1일

기본 완료 (예상)

2025년 5월 1일

연구 완료 (예상)

2025년 8월 1일

연구 등록 날짜

최초 제출

2019년 10월 11일

QC 기준을 충족하는 최초 제출

2019년 11월 1일

처음 게시됨 (실제)

2019년 11월 4일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2022년 10월 25일

QC 기준을 충족하는 마지막 업데이트 제출

2022년 10월 24일

마지막으로 확인됨

2022년 10월 1일

추가 정보

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이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

다발성 경화증에 대한 임상 시험

Fecal Microbial Transplants에 대한 임상 시험

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