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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04667884
Other study ID # 201911143
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 15, 2020
Est. completion date September 30, 2021

Study information

Verified date October 2021
Source Health Science Center of Xi'an Jiaotong University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study intends to evaluate the effects of three prebiotic solid beverages (mainly dietary fiber and prebiotics) and one probiotic solid beverage on the laxative effect of patients with functional constipation through randomized controlled trials. The influence of tract flora is expected to provide a basis for related therapies for patients with functional constipation.


Recruitment information / eligibility

Status Completed
Enrollment 250
Est. completion date September 30, 2021
Est. primary completion date May 22, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: 1. Adults: 18 to 70 years old (not less than 50% of the final population over 45 years old, and not less than 30% of men); 2. Patients with functional constipation (refer to Rome IV diagnostic criteria for functional constipation); * Symptoms appeared for at least 6 months before diagnosis, and met the above diagnostic criteria in the past 3 months Exclusion Criteria: 1. Pregnant and lactating women; 2. Unable to take the test sample and complete the inspection items as required due to inability to take food by mouth, weakness, allergies or other reasons (including the inability to complete all items due to recent travel plans); 3. Unclear main complaint and obvious abnormal mental state; 4. The liver and kidney function indexes are obviously abnormal (combined with the results of physical examination within the past 1 year); 5. Acute gastrointestinal diseases occurred in the past month, and constipation caused by surgical operations in the past month; 6. Take antibiotics, laxatives or topical agents, anticholinergics, antidiarrheals frequently in the past 1 month, and the frequency is more than 1 time/week 7. Have been diagnosed with the following diseases: cancer (especially cancer of the digestive tract), severe enteritis, intestinal obstruction, inflammatory bowel disease, hypothyroidism, mental illness; 8. Have been diagnosed with the following diseases: severe systemic diseases such as stroke, heart disease, liver cirrhosis, renal failure, hematopoietic system, or qualitative intestinal diseases caused by colonoscopy or imaging display; 9. In the past 3 months, there are often abdominal pain, abdominal pain accompanied by changes in bowel characteristics or frequency, blood in the stool, diarrhea or involuntary weight loss; 10. Clinical manifestations or diseases that other researchers believe are not suitable for participating in the project.

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Prebiotics or Probiotics
All the supplements were provided in solid drinks,and required to drink with plain water 35-40?, and lifestyle intervention was provided to all the groups by reading materials.

Locations

Country Name City State
China Xi'an Jiaotong University Xi'an Shaanxi

Sponsors (1)

Lead Sponsor Collaborator
Health Science Center of Xi'an Jiaotong University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of bowel movements per week bowel movements will be recorded per week week 0 to 4
Secondary Classification of bowel status Classification according to the difficulty of defecation 9/5000 According to the difficulty of defecation day 0, 14, 28
Secondary Bristol classification of stool characteristics Bristol classification day 0, 14, 28
Secondary glucose Fasting plasma day 0, 14, 28
Secondary HDL-C Fasting plasma day 0, 14, 28
Secondary LDL-C Fasting plasma day 0, 14, 28
Secondary TG Fasting plasma day 0, 14, 28
Secondary Tch Fasting plasma day 0, 14, 28
Secondary diversity and abundance of intestinal flora 16s rRNA day 0, 14, 28
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