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Clinical Trials/ITMCTR1900002644
ITMCTR1900002644
Not yet recruiting
Phase 1

A Multicenter, Randomized and Controlled Trial for Chang-An-Jun-Tai Granule in the Treatment of Patients With Irritable Bowel Syndrome With Diarrhea (IBS-D).

The First Affiliated Hospital of Guangzhou University of Traditional Chinese Medicine0 sitesTBD

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Irritable bowel syndrome
Sponsor
The First Affiliated Hospital of Guangzhou University of Traditional Chinese Medicine
Status
Not yet recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional study
Sex
All

Investigators

Sponsor
The First Affiliated Hospital of Guangzhou University of Traditional Chinese Medicine

Eligibility Criteria

Inclusion Criteria

  • To simultaneously satisfy the following criteria:
  • 1\. Conform to the Roman IV(Rome IV) of a patient diagnosed with IBS\-D and baseline IBS\-SSS score \> 75;
  • 2\. Aged 18 to 60 years;
  • 3\. Nearly 2 weeks no using the drugs in the treatment of IBS;
  • 4\. Nearly 2 weeks no using antibiotics or probiotics;
  • 5\. The patients volunteered to receive the drug and signed an informed consent form, and the informed consent process was in accordance with the relevant provisions of GCP.

Exclusion Criteria

  • Meet one of the following criteria were excluded:
  • 1\. there is explanation above the clinical symptoms of the patients with other diseases;
  • 2\. chronic esophagitis, Barrett esophagus and gastroesophageal reflux disease, peptic ulcer, gastric polyp (without resection), digestive tract tumor patients;
  • 3\. found that endoscopic gastric mucosa high grade intraepithelial neoplasia, pathological diagnosis, malignant gastrointestinal organic diseases;
  • 4\. patients with history of abdominal operation;
  • 5\. allergic or allergic to many medicines;
  • 6\. confusion, dementia, psychosis, neurosis and various serious unwilling to cooperate;
  • 7\. with serious the primary cardiovascular disease, liver disease, kidney disease, blood disease, lung disease, autoimmune diseases, or serious diseases affected the survival, such as cancer or aids;
  • 8\. pregnant and lactating women;
  • 9\. exist cognitive or other damage (such as vision, etc.) and impact on the participants completed self\-report;

Outcomes

Primary Outcomes

Not specified

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