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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04122586
Other study ID # 81774304
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date August 1, 2018
Est. completion date December 31, 2021

Study information

Verified date October 2019
Source Xiyuan Hospital of China Academy of Chinese Medical Sciences
Contact fengyun Wang, Ph.D
Phone +8601062835641
Email wfy811@163.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Diarrhea irritable bowel syndrome(IBS-D)has seriously affected health and quality of life of patients.It may be important pathogenesis in development and recurrence of the process of IBS-D,excessive endoplasmic reticulum stress (ERS) activated PERK(proteinkinaseR—like ERkinase,PERK)-eIF2a(eukaryotic translation initiation factor 2 alpha,eIF2a) pathway and damaged intestinal mucosal epithelial Barrier. Tongxieyaofang(TXYF) had obtained satisfactory effect in treating IBS-D in clinic and previous study, but it is unknown that herbal formula how to work.This project applies metabolomics method to detect plasma,urine and stool metabolites for patients before and after treatment, to determine the effects of the"multiple ingredients"of TXYF in body.


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date December 31, 2021
Est. primary completion date December 31, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- Patients meeting the diagnostic criteria of Western medicine for IBS-D;

- aged 18-70 years old; with a baseline IBS-SSS score over 75 points;

- voluntarily signed the informed consent;

- local resident who could ensure follow-ups, with basic reading ability

Exclusion Criteria:

- Patients with IBS-C, -M, and uncertain forms;

- accompanied with serious lesions in major organs including heart, liver, and kidney, hematopoietic system diseases, and tumors;

- gastrointestinal organic disease (e.g., chronic pancreatitis), or systemic diseases affecting the digestive tract motion (e.g., hyperthyroidism,diabetes, chronic renal insufficiency, and nervous system diseases);

- undergoing or requiring constant use of drugs that may affect gastrointestinal functions (e.g., anti-cholinergic drugs, calcium channel blockers, 5-HT3 receptor antagonist, antidiarrheal agents, antacids, prokinetic agents, antidepressants, anxiolytics, and intestinal flora regulating drugs);

- with history of abdominal surgery (e.g., cholecystectomy);

- with an allergy history of tested drugs or severe allergy history of food;

- pregnant and lactating female;

- with a history of neurological or psychiatric disorders;

- or participating in other clinical trial.

Study Design


Intervention

Drug:
Tongxieyaofang(granule)
Take this granule twice a day,one bag for each time,one hour after a meal,for 4 weeks

Locations

Country Name City State
China Xiyuan hospital Beijing Beijing

Sponsors (1)

Lead Sponsor Collaborator
Xiyuan Hospital of China Academy of Chinese Medical Sciences

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Irritable Bowel Syndrome Symptom Severity(IBS-SSS) scale Patients are graded according to their own symptoms(abdominal pain,bloating,defecation satisfaction,the extent to which the disease affects the lives of patients,bowel movements), the total score less than 75 points was considered as in remission, 75~175 as mild, 175~300 as moderate, and over 300 as severe. We will assess changes in patient scores before and after treatment to reflect the extent of disease remission. IBS-SSS was evaluated by patients at 4th week
Primary Bristol stool form scale(BSFS) Different fecal types can reflect different intestinal transit times, the lower the score, the longer the transmission time; the higher the score, the shorter the transmission time. We will assess changes in scores before and after treatment to reflect the extent of disease remission. BSFS was evaluated by patients at 4th week
Secondary IBS-D PRO( patient reported outcomes) Scale Grading from the field of physiology, independence, and psychology,Use score changes to assess improvement in all areas of the patient.Minimum score is 0,means no symptoms,maximum score is 144,means all symptoms are severe. IBS-D PRO Scale was evaluated at 4th week
Secondary SF-36(the MOS item short from health survey)Scale Score evaluation from 8 aspects: physical function, role-physical, pain, global health status, vitality,social function,role-emotional, mental health.Use score changes to assess improvement in all areas of the patient. Maximum score is147.The higher the score, the better the status in all aspects. SF-36 Scale was evaluated at 4th week