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临床试验/NCT06171126
NCT06171126进行中(未招募)不适用

The Role of Donor Selection on the Outcome of Faecal Microbiota Transplantation (FMT) in Patients With Irritable Bowel Syndrome: a Multi-center Randomised, Double-blinded Placebo-controlled Study

Haukeland University Hospital3 个研究点 分布在 1 个国家目标入组 500 人开始时间: 2024年2月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
500
试验地点
3
主要终点
Change in IBS-Severity Scoring System total score

研究概览

简要总结

Five hundred patients are randomized 1:1:1:1 into placebo (own feces), or receiving 90 g fecal transplant from donor A, donor B or donor C. The fecal transplant is administered to the distal duodenum via the working channel of a gastroscope. The patients shall complete 6 questionnaires measuring symptoms, fatigue, quality of life, stool form and diet intake at the baseline and at the end point of the trial and provide a feces sample at the baseline, and at 3, 6 and 12 months after FMT. Dysbiosis and fecal bacterial profile are determined by using 16S rRNA gene PCR DNA amplification/probe hybridization covering regions V3-V9.

详细描述

Study Description Brief Summary: Five hundred patients are randomized1:1:1:1 into placebo (own feces), receiving 90 g fecal transplant from donor A, donor B or donor C. The fecal transplant is administered to distal duodenum via working channel of a gastroscope. The patients shall complete 5 questionnaires measuring symptoms, fatigue, quality of life and diet intake at the baseline and at the end point of the trial and provide a feces sample at the baseline, and at 3, 6 and 12 months after FMT. Dysbiosis and fecal bacterial are determined by using 16S rRNA gene PCR DNA amplification/probe hybridization covering regions V3-V9.

Detailed Description: Patients: Five hundred patients who fulfil Rome IV criteria for irritable bowel syndrome (IBS) shall be included in the study. All IBS subtypes shall be included with the exception of IBS-U. Donors: The investigators have selected 3 donors (A, B and C) according to the criteria used in their previous randomised double-blind, placebo-controlled study. These criteria included: being a healthy man or woman with no history of disease and no use of medications, aged 20-50 years, being a non-smoker, and exercising regularly. They were borne by vaginal delivery and breastfed. They were treated only a few times with antibiotics during their life. They are screened according to the European guidelines for donors for FMT. Before they are accepted as donors, the bacterial profile and dysbiosis were analysed in a faecal sample using the GA-map dysbiosis test, with a dysbiosis index (DI)= 1, indicating normobiosis. Their feces shall be tested every third month during the trial to exclude communicable disease. Donor A is a male aged 41 years, donor B is a female aged 31 and donor C is a male aged 35.

Protocol: The patients are randomized 1:1:1:1 into placebo (to receive their own feces), to receive 90 g fecal transplant from donor A, from donor B or donor C. Fecal transplant is administered to the distal duodenum via the working channel of a gastroscope. The patients shall complete 5 questionnaires and deliver fecal samples at the baseline, and at 3 , 6 , and 12 months after FMT. Feces collection, preparation and administration: Faeces from both the donors and patients shall be collected and stored at - 80ºC. Frozen donor faeces shall be thawed in the refrigerator at 4ºC, and dissolved in 200 mL of 4ºC cold 0.9% sterile saline. The dissolved stool is administrated to the patients, after an overnight fast, through the working channel of a gastroduodenoscope in the pars descendens of the duodenum always distal to the papilla of Vater. Questionnaires

  1. IBS Symptom Severity Scale (IBS-SSS).
  2. Birmingham Symptom Scale.
  3. Fatigue Assessment Scale (FAS).
  4. IBS-quality of life (IBSQoL) Questionnaire.
  5. A 5-points subjective global assessment scale
  6. Bristol Stool Form Scale

Bacterial analysis: Fecal bacterial analysis is performed using a 16S rRNA gene PCR DNA amplification/probe hybridization technique covering regions V3-V9. DNA extraction is done by using magnetic beads. DI is based on 174 DNA probes targeting more than 300 bacterial strains based on their 16S rRNA sequence in seven variable regions (V3-V9). Probe labelling is by single nucleotide extension and hybridization to complementary probes coupled to magnetic beads, and signal detection by using BioCode 1000A 128-Plex Analyser (Applied BioCode, Santa Fe Springs, CA, USA). A DI above 2 shows a microbiota profile that differs from that of the normobiotic reference collection (DI 1-2: non-dysbiosis, DI: moderate, DI 4-5: severe dysbiosis).

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 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patients who fulfil Rome IV criteria for the
  • •diagnosis of IBS.
  • •Patients were investigated to exclude other
  • •gastrointestinal organic cause(s).
  • •Moderate-to-severe IBS symptoms, as indicated
  • •by a score of ≥175 on the IBS-SSS questionnaire

排除标准

  • •Pregnant, women planning pregnancy or lactating women.
  • •The use of antibiotics or probiotics within 1
  • •month prior to FMT.
  • •Having undergone any abdominal surgery, with
  • •the exception of appendectomy, cholecystectomy,
  • •caesarean section and hysterectomy.
  • •Previous treatment with FMT.
  • •Immunocompromised patients including those being
  • •treated by immunosuppressive medications.
  • •Patients with co-morbidity such as kidney failure,
  • •diabetes or chronic heart disease.
  • •Patients with serious psychiatric disorders
  • •or alcohol or drug abuse.

研究组 & 干预措施

Placebo

Placebo Comparator

Own faeces instilled to the small intestine during gastroscopy

干预措施: Placebo (Dietary Supplement)

Arm A

Experimental

90g of faeces from Donor A is instilled to the small intestine during gastroscopy

干预措施: Faeces from donor A (Dietary Supplement)

Arm B

Experimental

90g of faeces from Donor B is instilled to the small intestine during gastroscopy

干预措施: Faeces from donor B (Dietary Supplement)

Arm C

Experimental

90g of faeces from Donor C is instilled to the small intestine during gastroscopy

干预措施: Faeces from donor C (Dietary Supplement)

结局指标

主要结局

Change in IBS-Severity Scoring System total score

时间窗: 12 months after FMT

Irritable Bowel Syndrome-Severity Scoring System (IBS-SSS) is a visual analogue scale questionnaire with a total score between 0 and 500 points, with "0" meaning no symptom and higher scores meaning increasing severity. A decrease in total score by ≥50 points is considered as a meaningful response.

次要结局

  • Change in dysbiosis index(12 months after FMT)

研究者

发起方
Haukeland University Hospital
申办方类型
Other
责任方
Sponsor

研究点 (3)

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