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临床试验/CTRI/2024/01/062063
CTRI/2024/01/062063招募中2/3 期

Efficacy and Safety Of Oral Lyophilized Fecal Microbiome Capsules For Induction And Maintenance Of Remission In Moderately Severe Ulcerative Colitis

Vardhman Textiles Limited1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2024年2月1日最近更新:

试验速览

阶段
2/3 期
状态
招募中
发起方
入组人数
100
试验地点
1
主要终点
Clinical remission (defined as total Mayo score ≤2, with no individual sub-score exceeding 1 point)

研究概览

简要总结

Ulcerative colitis (UC) is a chronic, disabling immune mediated inflammatory condition affecting the large bowel, which is thought to be caused by an aberrant interaction between the immune system and a dysbiotic intestinal microbiome. There is emerging evidence that faecal microbiota transplantation (FMT) is effective in treating UC. This is a double blind, randomised, placebo-controlled trial of orally administered lyophilized FMT capsules in patients with chronic active UC.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant and Investigator Blinded

入排标准

年龄范围
18.00 Year(s) 至 75.00 Year(s)(—)
性别
All

入选标准

  • Patients of UC with active disease, defined as a total Mayo score of 6–9, and a Mayo endoscopic subscore of 1 or more.
  • Any disease extent : E1, E2 or E3
  • Diagnosis (endoscopic or radiographic and histological) of UC at least 6 months prior to enrolment into the study
  • Subjects who are willing and able to comply with treatment plan, laboratory tests.
  • Subjects who are willing to provide a written informed consent.

排除标准

  • Subjects without previous treatment for IBD (i.e. treatment-naïve).
  • Active or latent or inadequately treated infections(includingClostridiodes difficile, Cytomegalovirus, Mycobacterium tuberculosis, etc.)
  • Subjects displaying clinical signs of fulminant colitis or toxic megacolon.
  • Subjects infected with human immunodeficiency virus (HIV) or hepatitis B or C viruses.
  • Subjects with current malignancies or a past history of malignancies.
  • Subjects with current or recent history of severe, progressive, or uncontrolled renal, hepatic, haematological, gastrointestinal, metabolic, endocrine, pulmonary, cardiac, neurological disease.
  • Pregnant females.

结局指标

主要结局

Clinical remission (defined as total Mayo score ≤2, with no individual sub-score exceeding 1 point)

时间窗: Week 8, Week 48

次要结局

  • Clinical response (defined as decrease in total Mayo score by at least 3 points and at least 30%, with an accompanying decrease in the rectal bleeding sub-score of at least 1 point or absolute rectal bleeding sub-score of 0 or 1)(Week 8, Week 48)
  • Endoscopic remission (defined as endoscopic Mayo sub-score of 0)(Week 8, Week 48)

研究者

发起方
Vardhman Textiles Limited
申办方类型
Other [Corporate House]
责任方
Principal Investigator
主要研究者

Ajit Sood

Dayanand Medical College and Hospital, Ludhiana

研究点 (1)

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