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临床试验/CTRI/2026/01/102363
CTRI/2026/01/102363尚未招募3 期

Efficacy of bismuth quadruple therapy with bacillus clausii UBBC-07 and zinc carnosine for helicobacter pylori eradication: a double blind, parallel arm, randomized controlled trial

Unique Biotech Limited1 个研究点 分布在 1 个国家目标入组 170 人开始时间: 2026年3月1日最近更新:
适应症
相关药物

试验速览

阶段
3 期
状态
尚未招募
入组人数
170
试验地点
1
主要终点
Eradication rates of H. pylori in both the groups

研究概览

简要总结

Standard regimens for H. pylori infection typically involve triple or quadruple therapy. However, rising antibiotic resistance, adverse effects, and patient non-compliance significantly limit the success rates of these regimens. Probiotics have emerged as a promising adjunct or alternative strategy for H. pylori management. Among the wide strains of probiotics, Bacillus clausii has been shown to have a promising effect in reducing the side effects of H. pylori treatment, as previously studied . In another meta-analysis published in 2014, it is reported that probiotics formulated with specific Bacillus clausii strains are known to be more effective in eradicating H. pylori infection in patients. There are only a few studies on zinc carnosine-based modified bismuth quadruple therapy in H. pylori eradication, and no study has been reported in India yet. As an effective treatment for H. pylori infection, a probiotic formulated with zinc carnosine could be a significant factor in eradicating H. pylori in view of the very high antibiotic resistance reported from India to all first-line antibiotics. We hypothesize that administering probiotics during H. pylori eradication, based on limited available data, may mitigate adverse effects associated with the medication while simultaneously enhancing the eradication rate and compliance with the treatment. Further, safety data suggests it to be safe. Therefore, we aim to plan a randomized controlled trial to evaluate the role of Bacillus clausii UBBC-07 formulated with zinc carnosine in H. pylori eradication.

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 80.00 Year(s)(—)
性别
All

入选标准

  • Patients tested positive for H.
  • pylori on endoscopy by either RUT or HPE.
  • Written informed consent of the subject to participate.
  • PatientS above 18 years of age will be included in the study.

排除标准

  • Previous intolerance and/or adverse reactions to probiotics or the use of these products within the preceding 1 month.
  • Pregnancy or lactation.
  • Major systemic disease (e.g. heart failure, renal failure, malignant tumors, liver cirrhosis, etc.) Previous or current significant psychiatric co-morbidity Use of antibiotics in the preceding 1 month.
  • Patient on any specific diet.
  • Patient on any immunosuppressant drugs Patients who were unwilling to participate voluntarily in the study.

结局指标

主要结局

Eradication rates of H. pylori in both the groups

时间窗: Eradication rates of H. pylori in both the groups

次要结局

  • Overall adverse events(2 ,4 ,6 WEEKS)
  • Compliance of therapy(2 AND 4 WEEKS)
  • Changes in dyspeptic symptoms(2,4 AND 6 WEEKS)
  • Quality of Life(2,4 and 6 WEEKS)

研究者

申办方类型
Pharmaceutical industry-Indian
责任方
Principal Investigator
主要研究者

Dr Vaneet Jearth

Postgraduate Institute of Medical Education and Research

研究点 (1)

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