跳至主要内容
临床试验/CTRI/2024/07/070510
CTRI/2024/07/070510尚未招募Unknown

Observational study to assess efficacy and safety of Bifidobacterium longumW11 plus Fructooligosaccharide combination in patients with irritable bowel syndrome (IBS) - NI

Abbott India Ltd0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
Unknown
状态
尚未招募

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • Patients of either sex, aged between 18 and 60 years
  • OPD Patients with confirmed diagnosis of IBS with any of the three subtypes (viz IBS D/IBS C/IBS M)
  • Patients with no improvement in symptoms despite treatment with antispasmodics

排除标准

  • Patients will be excluded if they have severe respiratory insufficiency organic brain damage sleep apnea syndrome severe acute or chronic
  • hepatic insufficiency (risk of occurrence of encephalopathy) myasthenia gravis chronic psychosis major depressive episodes
  • phobic or obsessional states or dementia
  • Patients with other pre-existing GI disorders GI surgery abnormal upper and lower GI endoscopy finding family history of colon cancer or inflammatory bowel disease symptoms that discriminate lower GI organic diseases from IBS such as blood in stool nighttime symptoms
  • that cause sleep disturbance unintentional weight loss or change in typical IBS symptoms such as new and/or different pain and alcohol or drug-dependency

研究者

相似试验