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Exploratory Study on Dosage of Qizhi Weitong Granules in the Treatment of Irritable Bowel Syndrome (IBS)

C

China Resources Sanjiu Medical & Pharmaceutical

Status and phase

Unknown
Phase 2

Conditions

Irritable Bowel Syndrome

Treatments

Drug: Qizhi weitong granules(Low)
Drug: Placebo
Drug: Qizhi weitong granules(High)

Study type

Interventional

Funder types

Industry

Identifiers

NCT05113888
CR999-QZWT-IBS-01

Details and patient eligibility

About

The purpose of this study are as follows: 1) To evaluate the efficacy and safety of Qizhi Weitong granules in the treatment of diarrhea-type irritable bowel syndrome (IBS-D);2) To explore the dosage of Qizhi Weitong Granulesin treatment of IBS-D.

Enrollment

120 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • In line with the diagnostic criteria of WESTERN medicine IBS-D;
  • Aged 18-65 (including 18 and 65 years old) years;
  • The mean weekly NRS score for abdominal pain (the most severe in the past 24 hours) was between 3.0 and 7.0 within the last week, and there were at least 2 days per week when fecal traits were classified as type 6 or 7;
  • Informed consent, voluntary test.

Exclusion criteria

  • Stool number of type 7 according to Bristol Stool Chart, more than 3 times per day;
  • TCM syndrome was diagnosed as deficiency of spleen and kidney Yang syndrome;
  • Patients who took emergency medication (Piveronium bromide tablets) more than the standard during admission period (more than 2 days per week on average);
  • Patients who have been diagnosed with organic diseases of digestive system, such as inflammatory bowel disease, intestinal tuberculosis, intestinal tumor, etc., or are still complicated with peptic ulcer and infectious diarrhea;
  • Patients with similar symptoms of IBS, such as eosinophilic enteritis, collagenous enteritis, lactose intolerance, etc.
  • Patients with intestinal diseases of digestive system, such as tuberculous peritonitis, cirrhosis, chronic pancreatitis, etc.
  • Patients with systemic diseases affecting digestive tract function, such as hyperthyroidism or hypothyroidism, endometriosis, chronic renal insufficiency, autoimmune diseases, diabetes, etc.
  • Previous gastrointestinal surgery (except for appendicitis);
  • Patients with serious cardiovascular diseases, serious liver and kidney diseases, hematopoietic system diseases, tumor, neurological or psychiatric system diseases;
  • Major anxiety (SAS score ≥70) or major depression (SDS Score ≥73);
  • Concomitant drugs affecting gastrointestinal motility and function (prokinetic drugs, anticholinergic drugs, calcium channel blockers, 5-HT3 receptor antagonists, antidiarrhea agents, antacids, antidepressants, antianxiety drugs, intestinal microbiota regulators, antibiotics, etc.) should not be discontinued in the test;
  • Pregnant or lactating women who had a birth plan from enrollment to 3 months after the end of the trial.
  • Allergic to the test drug emergency drug and its ingredients;
  • Suspected or confirmed history of alcohol or drug abuse;
  • Patients who participated in other clinical trials within 1 month prior to enrollment;
  • Other subjects considered unsuitable for clinical trials by the researchers.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

120 participants in 3 patient groups, including a placebo group

Qizhi Weitong granules high-dose group
Experimental group
Description:
interventions:Qizhi Weitong granules Specification: 5.0g/bag,the drug content is equivalent to 2 bags of Qizhi Weitong granules (2.5g/ bag commercially available).
Treatment:
Drug: Qizhi weitong granules(High)
Qizhi Weitong granules low-dose group
Experimental group
Description:
interventions:Qizhi Weitong granules Specification: 5.0g/bag,the drug content is equivalent to 1 bag of Qizhi Weitong granules (2.5g/ bag commercially available).
Treatment:
Drug: Qizhi weitong granules(Low)
The control group
Placebo Comparator group
Description:
interventions:Qizhi Weitong granules placebo Specification: 5.0g/bag,Does not contain effective crude drug ingredients.
Treatment:
Drug: Placebo

Trial contacts and locations

0

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Central trial contact

Xudong Tang, professor

Data sourced from clinicaltrials.gov

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